Monoclonal Antibody to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

ABC35; ABCC7; CF; CFTR/MRP; MRP7; TNR-CFTR; ATP-Binding Cassette Subfamily C,Member 7; Channel conductance-controlling ATPase; cAMP-dependent chloride channel

  • Monoclonal Antibody to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Packages (Simulation)
  • Monoclonal Antibody to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Packages (Simulation)
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

SPECIFITY of the Monoclonal Antibody to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

The antibody is a mouse monoclonal antibody raised against CFTR. It has been selected for its ability to recognize CFTR in immunohistochemical staining and western blotting.

USAGE of the Monoclonal Antibody to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Western blotting: 0.01-2µg/mL;
Immunohistochemistry: 5-20µg/mL;
Immunocytochemistry: 5-20µg/mL;
Optimal working dilutions must be determined by end user.

STORAGE of the of the Monoclonal Antibody to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Store at 4°C for frequent use. Stored at -20°C in a manual defrost freezer for two year without detectable loss of activity. Avoid repeated freeze-thaw cycles.

STABILITY of the Monoclonal Antibody to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.

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