Modelli animali sperimentali suggeriscono che l’acido urico potrebbe avere un ruolo patogeno nello sviluppo precoce dell’ipertensione primaria. Abbiamo ipotizzato che l’acido urico sierico sia correlato alla pressione sanguigna nei bambini con ipertensione primaria di nuova insorgenza, non trattata. Abbiamo valutato 125 bambini consecutivi inviati al programma renale pediatrico Baylor per la valutazione dell’ipertensione. Nessuno dei soggetti era stato precedentemente valutato o trattato per l’ipertensione. I bambini avevano un’età compresa tra 6 e 18 anni (media, 13,4 +/- 3,3) e avevano una normale funzione renale (clearance della creatinina> 80 mL x min (-1) x 1,73 m (-2)).
Sessantatré bambini avevano ipertensione primaria, 40 avevano ipertensione secondaria e 22 avevano ipertensione da camice bianco. Quaranta controlli con pressione sanguigna normale sono stati reclutati dalla clinica renale. I livelli di acido urico erano direttamente correlati con la pressione sanguigna sistolica (r = 0,80, P = 0,0002) e diastolica (r = 0,66, P = 0,0006) nei controlli e nei soggetti con ipertensione primaria ed erano indipendenti dalla funzione renale. Concentrazioni sieriche di acido urico> 5,5 mg / dL sono state trovate nell’89% dei soggetti con ipertensione primaria, nel 30% con ipertensione secondaria, nello 0% con ipertensione da camice bianco e nello 0% dei controlli.
Concludiamo che l’acido urico sierico è direttamente correlato alla pressione sanguigna nei bambini non trattati e che un valore di acido urico sierico> 5,5 mg / dL in un adolescente valutato per l’ipertensione suggerisce fortemente l’ipertensione primaria rispetto all’ipertensione da camice bianco o secondaria. Questi risultati sono coerenti con l’ipotesi che l’acido urico possa avere un ruolo nella patogenesi precoce dell’ipertensione primaria.
Fourteen questions from the Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present Episode (K-SADS-P) 1986 version plus a new item assessing mood lability were used to construct a clinician-rated mania rating scale (K-SADS-MRS). Interrater reliability was determined prospectively with 22 patients from a bipolar outpatient clinic. Sensitivity to treatment effects was determined in a separate cohort of 23 patients.
Valutazione funzionale dei pazienti pediatrici con dolore: proprietà psicometriche dell’inventario della disabilità funzionale.
L’inventario della disabilità funzionale (FDI; Walker LS, Greene JW. L’inventario della disabilità funzionale: misurazione di una dimensione trascurata dello stato di salute del bambino. J Pediatr Psychol 1991; 16: 39-58) valuta le limitazioni dell’attività in bambini e adolescenti con una varietà di pediatria condizioni. Questo studio ha valutato le proprietà psicometriche dell’FDI nei pazienti pediatrici con dolore. I partecipanti includevano 596 pazienti con dolore addominale cronico, di età compresa tra 8 e 17 anni, e un sottogruppo dei loro genitori (n = 151) che hanno completato l’FDI e le misure di dolore, limitazioni nelle attività scolastiche e sintomi somatici e depressivi durante una visita clinica.
L’affidabilità del test-retest era alta a 2 settimane (rapporto del bambino, .74; rapporto del genitore, .64) e moderato a 3 mesi (rapporto del bambino, .48; rapporto del genitore, .39). L’affidabilità della coerenza interna è stata eccellente, con un range da .86 a .91. La validità è stata supportata da correlazioni significative dei punteggi FDI riportati da genitori e figli con misure di disabilità, dolore e sintomi somatici legati alla scuola. I risultati dello studio si aggiungono a un corpo crescente di letteratura empirica a supporto dell’affidabilità e della validità dell’FDI per la valutazione funzionale dei pazienti pediatrici con dolore cronico.
L’esposizione alle spore disperse nell’aria della muffa comune Alternaria alternata è stata implicata negli attacchi di asma. Tale esposizione è particolarmente frequente nel Midwest durante i mesi estivi e autunnali. Per determinare il ruolo di A. alternata nell’innescare gravi attacchi di asma, abbiamo studiato i casi di 11 pazienti con asma che avevano avuto un arresto respiratorio improvviso e determinato la frequenza di sensibilità a questo allergene in questi pazienti.

Consegna genica sistemica in specie di grandi dimensioni per il targeting del midollo spinale, del cervello e dei tessuti periferici per i disturbi pediatrici.
Il virus adeno-associato di tipo 9 (AAV9) è un potente strumento per il rilascio di geni in tutto il sistema nervoso centrale (SNC) dopo l’iniezione endovenosa. I risultati preclinici nei modelli pediatrici di atrofia muscolare spinale (SMA) e disturbi da accumulo lisosomiale forniscono un caso convincente per portare l’AAV9 alla clinica. Un passo importante della traduzione è dimostrare un efficiente targeting del sistema nervoso centrale in animali di grandi dimensioni di varie età. Nel presente studio, abbiamo testato AAV9 iniettato sistemicamente in macachi cynomolgus, somministrato alla nascita fino ai 3 anni di età per il targeting del sistema nervoso centrale e dei tessuti periferici.
Mostriamo che AAV9 era efficiente nell’attraversare la barriera emato-encefalica (BBB) in tutti i punti temporali studiati. L’espressione del transgene è stata rilevata principalmente nelle cellule gliali in tutto il cervello, nei neuroni dei gangli della radice dorsale e nei neuroni motori all’interno del midollo spinale, fornendo fiducia per la traduzione ai pazienti SMA. L’iniezione sistemica ha anche mirato efficacemente ai muscoli scheletrici e agli organi periferici.
Eye Lysate (0 Days Old) |
1420-0 |
ProSci |
0.1 mg |
EUR 191 |
Description: Eye tissue lysate (0 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Heart Lysate (0 day old mouse) |
1401-0 |
ProSci |
0.1 mg |
EUR 191 |
Description: Heart tissue lysate (0 day old mouse) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Human Fecal calprotectin(fecal calprotectin) ELISA Kit |
QY-E05394 |
Qayee Biotechnology |
96T |
EUR 361 |
Rabbit Serum Sterile, trace-hemolized (56-84 days old) |
31126-3 |
Pel-Freez |
3L |
EUR 694 |
|
Description: Produced from whole blood collected from young healthy rabbits (New Zealand White or Californian), 6+ months old. Pooled serum from male and female rabbits that are fasted prior to collection. The serum is processed, bottled, and stored at -20°C. Then the serum was thawed, pooled, passed through a 0.22-micron filter, bottled and returned to -20°C. |
Antibody analysis - human >30 samples |
8005-3 |
Chondrex |
Custom service |
EUR 113.8 |
Description: Antibody analysis - human >30 samples |
RealScreen Pediatric FSH ELISA Kit |
EL103-096 |
GenDepot |
96T |
EUR 1832 |
ISOLATE Fecal DNA Kit |
BIO-52038 |
Bioline |
100 preps (Kit 2 x 50 preps) |
Ask for price |
ISOLATE Fecal DNA Kit |
BIO-52082 |
Bioline |
50 preps |
Ask for price |
AGEs-BSA |
KH001-A |
Sceti |
|
EUR 870 |
Description: The AGEs-BSA is available in Europe and for worldwide shipping via Gentaur. |
Rabbit Complement 3-4 WK (1-mL) |
31061-0 |
Pel-Freez |
1mL |
EUR 93.28 |
Hemoglobin Fecal Occult Blood (FOB) Antibody |
abx024027-1mg |
Abbexa |
1 mg |
EUR 829 |
|
Hemoglobin Fecal Occult Blood (FOB) Antibody |
abx024028-1mg |
Abbexa |
1 mg |
EUR 829 |
|
Sheep AGEs ELISA Kit |
ESA0009 |
Abclonal |
96Tests |
EUR 521 |
Mouse AGEs ELISA Kit |
EMA0009 |
Abclonal |
96Tests |
EUR 521 |
Monkey AGEs ELISA Kit |
EMKA0009 |
Abclonal |
96Tests |
EUR 521 |
Porcine AGEs ELISA Kit |
EPA0009 |
Abclonal |
96Tests |
EUR 521 |
Rat AGEs ELISA Kit |
ERA0009 |
Abclonal |
96Tests |
EUR 521 |
Rabbit AGEs ELISA Kit |
ERTA0009 |
Abclonal |
96Tests |
EUR 521 |
Anserini AGEs ELISA Kit |
EAA0009 |
Abclonal |
96Tests |
EUR 521 |
Goat AGEs ELISA Kit |
EGTA0009 |
Abclonal |
96Tests |
EUR 521 |
Chicken AGEs ELISA Kit |
ECKA0009 |
Abclonal |
96Tests |
EUR 521 |
Bovine AGEs ELISA Kit |
EBA0009 |
Abclonal |
96Tests |
EUR 521 |
34011-0 Human Serum Off Clot Single Donor (1mL) |
34011-1 |
Pel-Freez |
1mL |
EUR 68.81 |
Rabbit BRAIN ACETONE POWDER VARISENS (1-g) |
41170-0 |
Pel-Freez |
1g |
EUR 104.15 |
Heart Lysate (14 Days Old) |
1401-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Heart tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Lung Lysate (14 Days Old) |
1402-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Lung tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Lung Lysate (7 Days Old) |
1402-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Lung tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Brain Lysate (14 Days Old) |
1403-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Brain tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Brain Lysate (7 Days Old) |
1403-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Brain tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Liver Lysate (14 Days Old) |
1404-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Liver tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Liver Lysate (7 Days Old) |
1404-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Liver tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Kidney Lysate (14 Days Old) |
1405-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Kidney tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Kidney Lysate (7 Days Old) |
1405-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Kidney tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Spleen Lysate (14 Days Old) |
1406-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Spleen tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Spleen Lysate (7 Days Old) |
1406-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Spleen tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Thymus Lysate (14 Days Old) |
1409-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Thymus tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Thymus Lysate (7 Days Old) |
1409-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Thymus tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Stomach Lysate (14 Day Old) |
1415-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Stomach tissue lysate (14 Day Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Stomach Lysate (7 Day Old) |
1415-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Stomach tissue lysate (7 Day Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Skin Lysate (14 Days Old) |
1419-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Skin tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Skin Lysate (7 Days Old) |
1419-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Skin tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Eye Lysate (14 Days Old) |
1420-14 |
ProSci |
0.1 mg |
EUR 191 |
Description: Eye tissue lysate (14 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Eye Lysate (7 Days Old) |
1420-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Eye tissue lysate (7 Days Old) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
Yersinia Enterocolitica 0:3 Protein |
abx061492-01ml |
Abbexa |
0.1 ml |
EUR 551 |
|
Guinea Pig AGEs ELISA Kit |
EGA0009 |
Abclonal |
96Tests |
EUR 521 |
Mouse Aquaporin 0(AQP-0)ELISA Kit |
GA-E0524MS-48T |
GenAsia Biotech |
48T |
EUR 336 |
Mouse Aquaporin 0(AQP-0)ELISA Kit |
GA-E0524MS-96T |
GenAsia Biotech |
96T |
EUR 534 |
Human Aquaporin 0(AQP-0)ELISA Kit |
GA-E1301HM-48T |
GenAsia Biotech |
48T |
EUR 289 |
Human Aquaporin 0(AQP-0)ELISA Kit |
GA-E1301HM-96T |
GenAsia Biotech |
96T |
EUR 466 |
Human Aquaporin 0,AQP-0 ELISA Kit |
201-12-1285 |
SunredBio |
96 tests |
EUR 440 |
|
Description: A quantitative ELISA kit for measuring Human in samples from biological fluids. |
Rat Aquaporin 0,AQP-0 ELISA Kit |
CN-01885R1 |
ChemNorm |
96T |
EUR 471 |
Rat Aquaporin 0,AQP-0 ELISA Kit |
CN-01885R2 |
ChemNorm |
48T |
EUR 322 |
Mouse Aquaporin 0,AQP-0 ELISA Kit |
CN-02762M1 |
ChemNorm |
96T |
EUR 464 |
Mouse Aquaporin 0,AQP-0 ELISA Kit |
CN-02762M2 |
ChemNorm |
48T |
EUR 313 |
Human Aquaporin 0,AQP-0 ELISA Kit |
CN-04417H1 |
ChemNorm |
96T |
EUR 464 |
Human Aquaporin 0,AQP-0 ELISA Kit |
CN-04417H2 |
ChemNorm |
48T |
EUR 313 |
Rat Aquaporin 0,AQP-0 ELISA kit |
E02A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Rat Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Rat Aquaporin 0,AQP-0 ELISA kit |
E02A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Rat Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Rat Aquaporin 0,AQP-0 ELISA kit |
E02A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Rat Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Dog Aquaporin 0,AQP-0 ELISA kit |
E08A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Canine Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Dog Aquaporin 0,AQP-0 ELISA kit |
E08A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Canine Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Dog Aquaporin 0,AQP-0 ELISA kit |
E08A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Canine Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Rabbit Aquaporin 0,AQP-0 ELISA kit |
E04A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Rabbit Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Rabbit Aquaporin 0,AQP-0 ELISA kit |
E04A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Rabbit Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Rabbit Aquaporin 0,AQP-0 ELISA kit |
E04A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Rabbit Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Monkey Aquaporin 0,AQP-0 ELISA kit |
E09A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Monkey Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Monkey Aquaporin 0,AQP-0 ELISA kit |
E09A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Monkey Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Monkey Aquaporin 0,AQP-0 ELISA kit |
E09A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Monkey Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Mouse Aquaporin 0,AQP-0 ELISA kit |
E03A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Mouse Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Mouse Aquaporin 0,AQP-0 ELISA kit |
E03A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Mouse Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Mouse Aquaporin 0,AQP-0 ELISA kit |
E03A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Mouse Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Pig Aquaporin 0,AQP-0 ELISA kit |
E07A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Porcine Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Pig Aquaporin 0,AQP-0 ELISA kit |
E07A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Porcine Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Pig Aquaporin 0,AQP-0 ELISA kit |
E07A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Porcine Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Goat Aquaporin 0,AQP-0 ELISA kit |
E06A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Goat Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Goat Aquaporin 0,AQP-0 ELISA kit |
E06A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Goat Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Goat Aquaporin 0,AQP-0 ELISA kit |
E06A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Goat Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Human Aquaporin 0,AQP-0 ELISA kit |
E01A1918-192T |
BlueGene |
192 tests |
EUR 1270 |
|
Description: A sandwich ELISA for quantitative measurement of Human Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Human Aquaporin 0,AQP-0 ELISA kit |
E01A1918-48 |
BlueGene |
1 plate of 48 wells |
EUR 520 |
|
Description: A sandwich ELISA for quantitative measurement of Human Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Human Aquaporin 0,AQP-0 ELISA kit |
E01A1918-96 |
BlueGene |
1 plate of 96 wells |
EUR 685 |
|
Description: A sandwich ELISA for quantitative measurement of Human Aquaporin 0,AQP-0 in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
Heart Lysate (7 day old mouse) |
1401-7 |
ProSci |
0.1 mg |
EUR 191 |
Description: Heart tissue lysate (7 day old mouse) was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
ELISA kit for Mouse AQP-0 (Aquaporin 0) |
E-EL-M0144 |
Elabscience Biotech |
1 plate of 96 wells |
EUR 534 |
|
Description: A sandwich ELISA kit for quantitative measurement of Mouse AQP-0 (Aquaporin 0) in samples from Serum, Plasma, Cell supernatant |
ELISA kit for Human Aquaporin 0 (AQP-0) |
KTE61608-48T |
Abbkine |
48T |
EUR 354 |
|
Description: Quantitative sandwich ELISA for measuring Human Aquaporin 0 (AQP-0) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
ELISA kit for Human Aquaporin 0 (AQP-0) |
KTE61608-5platesof96wells |
Abbkine |
5 plates of 96 wells |
EUR 2252 |
|
Description: Quantitative sandwich ELISA for measuring Human Aquaporin 0 (AQP-0) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
ELISA kit for Human Aquaporin 0 (AQP-0) |
KTE61608-96T |
Abbkine |
96T |
EUR 572 |
|
Description: Quantitative sandwich ELISA for measuring Human Aquaporin 0 (AQP-0) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
ELISA kit for Rat Aquaporin 0 (AQP-0) |
KTE100611-48T |
Abbkine |
48T |
EUR 354 |
|
Description: Quantitative sandwich ELISA for measuring Rat Aquaporin 0 (AQP-0) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids. |
Per mirare specificamente al sistema nervoso centrale, abbiamo esplorato la consegna di AAV9 al liquido cerebrospinale (CSF). L’iniezione di CSF ha mirato efficacemente ai motoneuroni e ha limitato l’espressione genica al sistema nervoso centrale, fornendo un percorso di consegna alternativo e requisiti di produzione potenzialmente inferiori per i pazienti più grandi e più grandi. I nostri risultati supportano l’uso di AAV9 per il trasferimento genico al sistema nervoso centrale per i disturbi nelle popolazioni pediatriche.