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Invitrogen™ CFTR Polyclonal Antibody
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Goat Polyclonal Antibody

Supplier:  Invitrogen™ PA5142139

Catalog No. PIPA5142139


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Description

Description

This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:32,000.

Cystic Fibrosis (CF) is a common lethal genetic disease caused by mutations of the gene coding for the cystic fibrosis transmembrane conductance factor, a cAMP regulated chloride channel. Approximately 70% of all CF cases share the deletion of a phenylalanine at position 508 (delta F508) which results in abnormal chloride transport. Since the CF mutation is lethal, most often by lung and liver disease, it raises the question of why this genetic disease remains as common as it is. One possible explanation is that Salmonella typhi has been shown to use CFTR to enter intestinal epithelial cells and that delta F508 heterozygote and homozygote mice showed 86% and 100% reductions in S. typhi intestinal submucosal uptake.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

CFTR
Polyclonal
Unconjugated
CFTR
ABC35; Abcc7; ATP Binding Cassette Superfamily C Member 7 (ABCC7); ATP-binding cassette sub-family C member 7; ATP-binding cassette transporter sub-family C member 7; ATP-binding cassette, subfamily c, member 7; AW495489; cAMP-dependent chloride channel; CF; CFTR; CFTR/MRP; Channel conductance-controlling ATPase; cystic fibrosis transmembrane conductance regulator; cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7); cystic fibrosis transmembrane conductance regulator homolog; cystic fibrosis transmembrane conductance regulator homolog; ATP-binding cassette, subfamily c, member 7; dJ760C5.1; MRP7; RGD1561193; tcag7.78; TNR CFTR; TNR-CFTR
Goat
Ammonium Sulfate Precipitation
RUO
1080
-20°C, Avoid Freeze/Thaw Cycles
Liquid
Immunohistochemistry (Paraffin)
0.5 mg/mL
TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3
P13569
CFTR
Peptide with sequence QRSPLEKASVVSK-C (aa 2-14).
100 μg
Primary
Human
Antibody
IgG
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