- ￥13338
- Biorbyt
- orb1252187
- 英国
- 2026年07月31日
- IF, IHC-P, WB
- Mouse
- Human
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- 文献和实验
- 技术资料
- 抗体名：
CFTR Antibody 抗体
- 抗体英文名：
CFTR Antibody
- 靶点：
CFTR
- 浓度：
0.2 mg/mL
- 应用范围：
IF, IHC-P, WB
- 宿主：
Mouse
- 适应物种：
Human
- 保质期：
12 months from date of receipt.
- 抗原来源：
详询
- 目录编号：
orb1252187
- 级别：
科研
- 库存：
99
- 供应商：
Biorbyt
- 标记物：
Unconjugated
- 克隆性：
Monoclonal
- 保存条件：
详询
- 形态：
Liquid
- 亚型：
IgG1
- 免疫原：
详询
- 规格：
100 ug
产品子类型: Primary Antibody
描述: CFTR Antibody
克隆号: CFTR/1341
别名: CFTR Antibody: CF, MRP7, ABC35, ABCC7, CFTR/MRP, TNR-CFTR, dJ760C5.1, Cystic fibrosis transmembrane conductance regulator, ATP-binding cassette sub-family C member 7, CFTR
应用说明: Immunofluorescence: 1-2 µg/mLWestern blot: 0.5-1 µg/mLIHC (FFPE): 0.5-1 µg/mL for 30 min at RTThe concentration stated for each application is a general starting point. Variations in protocols, secondaries and substrates may require the CFTR antibody to be titered up or down for optimal performance.
免疫原: Human recombinant protein was used as the immunogen for this CFTR antibody.
防腐剂: PBS with 0.1 mg/ml rAlbumin and 0.05% sodium azide
纯化方法: Protein G affinity chromatography
研究领域: Cell Biology
UniProt ID: P13569
保存条件: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
备注: For research use only.
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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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