Lab Reagents
Human Elisa Laboratories manufactures the human cftr elisa kit on cell surface reagents distributed by Genprice. The Human Cftr Elisa Kit On Cell Surface reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Human elisa. Other Human products are available in stock. Specificity: Human Category: Cftr Group: Elisa Kit
Elisa Kit information
Rat Osteonectin (ON) ELISA Kit |
RDR-ON-Ra-48Tests |
Reddot Biotech |
48 Tests |
EUR 640.8 |
Rat Osteonectin (ON) ELISA Kit |
RDR-ON-Ra-96Tests |
Reddot Biotech |
96 Tests |
EUR 890.4 |
QuickTiter Hepatitis B Surface Antigen (HBsAg) ELISA Kit |
VPK-5004 |
Cell Biolabs |
96 assays |
EUR 1096.8 |
Description: The QuickTiter Hepatitis B Surface Antigen ELISA Kit measures HBsAg with sensitivity as low as 1 ng/mL. Reagents are sufficient for 96 wells including standards and unknown samples. |
QuickTiter Hepatitis B Surface Antigen (HBsAg) ELISA Kit |
VPK-5004-5 |
Cell Biolabs |
5 x 96 assays |
EUR 4507.2 |
Description: The QuickTiter Hepatitis B Surface Antigen ELISA Kit measures HBsAg with sensitivity as low as 1 ng/mL. Reagents are sufficient for 5x96 wells including standards and unknown samples. |
Human CFTR ELISA Kit |
EHC0458 |
Abclonal |
96Tests |
EUR 625.2 |
Human CFTR ELISA Kit |
STJ150459 |
St John's Laboratory |
1 kit |
EUR 494.4 |
Description: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of CFTR in human serum, plasma and other biological fluids |
CFTR ELISA Kit (Human) (OKAN06120) |
OKAN06120 |
Aviva Systems Biology |
96 Wells |
EUR 950.4 |
Description: Description of target: This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.059 ng/mL |
CFTR ELISA Kit (Human) (OKCD08127) |
OKCD08127 |
Aviva Systems Biology |
96 Wells |
EUR 1170 |
Description: Description of target: This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. The encoded protein functions as a chloride channel, making it unique among members of this protein family, and controls ion and water secretion and absorption in epithelial tissues. Channel activation is mediated by cycles of regulatory domain phosphorylation, ATP-binding by the nucleotide-binding domains, and ATP hydrolysis. Mutations in this gene cause cystic fibrosis, the most common lethal genetic disorder in populations of Northern European descent. The most frequently occurring mutation in cystic fibrosis, DeltaF508, results in impaired folding and trafficking of the encoded protein. Multiple pseudogenes have been identified in the human genome.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.059ng/mL |
CFTR ELISA Kit (Human) (OKDD00186) |
OKDD00186 |
Aviva Systems Biology |
96 Wells |
EUR 1170 |
Description: Description of target: This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily that is involved in multi-drug resistance. The encoded protein functions as a chloride channel and controls the regulation of other transport pathways. Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens. Alternatively spliced transcript variants have been described, many of which result from mutations in this gene.;Species reactivity: Human;Application: ;Assay info: Quantitative Sandwich ELISA;Sensitivity: < 0.053 ng/mL |
Human ON ELISA Kit |
EHO0024 |
Abclonal |
96Tests |
EUR 625.2 |
Mouse CFTR ELISA Kit |
EMC0458 |
Abclonal |
96Tests |
EUR 625.2 |
Sheep CFTR ELISA Kit |
ESC0458 |
Abclonal |
96Tests |
EUR 625.2 |