- 询价
- Signalway Antibody
- USA
- 13077
- 2025年07月09日
- WB
- Rabbit
- Hu, Ms, Rt
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
A synthesized peptide derived from human CFTR around the phosphorylation site of Thr1471
- 形态：
liquid
- 保存条件：
Store at -20˚C
- 克隆性：
Polyclonal
- 适应物种：
Hu, Ms, Rt
- 宿主：
Rabbit
- 应用范围：
WB
- 浓度：
1mg/ml
- 抗体英文名：
CFTR (Phospho-Thr1471) Antibody
clonality:Polyclonal
specificity:Phospho-CFTR (Phospho-Thr1471) Antibody detects endogenous levels of CFTR only when phosphorylated at Thr1471
other_names:ABC 35; ABC35; ABCC 7; ABCC7; ATP binding cassette sub family C member 7; ATP Binding Cassette Superfamily C Member 7; ATP binding cassette transporter sub family C member 7; ATP-binding cassette sub-family C member 7; cAMP dependent chloride channel; cAMP-dependent chloride channel; CF; CFTR; CFTR/MRP; CFTR_HUMAN; Channel conductance controlling ATPase; Channel conductance-controlling ATPase; Cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub family C, member 7); Cystic fibrosis transmembrane conductance regulator; Cystic fibrosis transmembrane conductance regulator ATP binding cassette sub family C member 7; Cystic Fibrosis Transmembrane Regulator; dJ760C5.1; MRP 7; MRP7; TNR CFTR; accession_no:Swiss-Prot#:P13569
NCBI Gene ID:1080
产品详细信息请点击：CFTR (Phospho-Thr1471) Antibody
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文献和实验CFTR Folding Consortium: Methods Available for Studies of CFTR Folding and Correction
of expressed HA-tagged CFTR by ELISA and (b) the generation and use of an antibody to CFTR’s first extracellular loop for the detection of endogenous CFTR. Finally, we highlight a systematic collection of assays, the CFC Roadmap, which is being used to assess
Immunolocalization of CFTR in Intact Tissue and Cultured Cells
Cloning of the cystic fibrosis (CF) gene provided, for the first time, the structural information needed to more precisely define the CF defect (1 -3 ). This genetic information was used to develop powerful molecular and antibody reagents
Antibody Microarrays: Analysis of Cystic Fibrosis
proinflammatory condition in the lung. The mutation responsible for most cases of CF is [ΔF508]CFTR. However, the penetrance of the disease is quite variable, and adverse events leading to hospitalization cannot be easily predicted. Thus, there is a strong
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