CFTR Rabbit Polyclonal Antibody

CAT#: AP10443PU-N

CFTR rabbit polyclonal antibody, Purified

Product Images

BHK cells expressing wild-type (wt) CFTR or mutated (rΔF508) CFTR, were fixed, permeabilized, and CFTR protein was detected with the specific anti-CFTR antibody .

Specifications

Product Data

• Applications: ELISA, IF, IP, WB
• Recommended Dilution: ELISA: 1/2000-1/32000.
  Western Blot: 1/500-1/1000.
  Immunofluorescence.
  Immunoprecipitation.
• Reactivities: Human
• Host: Rabbit
• Clonality: Polyclonal
• Immunogen: Synthetic peptide derived from Cter domain of human CFTR protein.
• Specificity: Reacts with Human 168 kDa CFTR.
• Formulation: 0.1M Tris 0.1M Glycine, 2% Sucrose
  State: Purified
  State: Lyophilized purified antibody
  Preservative: None
• Concentration: lot specific
• Purification: Affinity Chromatography on Protein A
• Conjugation: Unconjugated
• Storage: Store lyophilized at 2-8°C for 6 months or at -20°C long term.
  After reconstitution store the antibody undiluted at 2-8°C for one month
  or (in aliquots) at -20°C long term.
  Avoid repeated freezing and thawing.
• Stability: Shelf life: one year from despatch.
• Gene Name: cystic fibrosis transmembrane conductance regulator
• Database Link:
  Entrez Gene 1080 Human
  UniProt ID P13569
• Background: Cystic Fibrosis (CF) is a common lethal genetic disease characterized by chronic bronchopulmonary disease, elevated sweat electrolytes and insufficient pancreatic function. CF is caused by mutations of the CFTR gene, which encodes the cystic fibrosis transmembrane conductance regulator (CFTR). The CFTR protein is a cAMP-activated chloride channel found in the apical membranes of epithelia within the pancreas, airway, intestine, bile duct, sweat gland, and male genital ducts. Approximately 70% of all CF cases share the deletion of a phenylalanine at position 508 which results in abnormal chloride transport. CFTR is structurally similar to multi-drug resistance (Mdr1) protein and both are members of the superfamily of ATP-binding cassette (ABC) transporters. CFTR is a valuable marker of human pancreatic duct cell development and differentiation.
• Synonyms: Cystic fibrosis transmembrane conductance regulator