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Polyclonal Antibody to Homo sapiens (Human) 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

Description: Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Source:Polyclonal antibody preparation

Host: Rabbit

Reactivity: Homo sapiens (Human)

Isotype: IgG

Purification: Antigen-specific affinity chromatography

Label: None

Buffer Formulation: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.

Form Supplied: Liquid

Concentration: 200ug/ml

Tested Applications:

  • Western blot (1:100 to 1:500)
  • Immunofluorescence (1:50 to 1:400)
  • Immunohistochemistry (1:200 to 1:500)
  • Flow cytometry analysis (1:200 to 1:500)
  • Enzyme-linked Immunosorbent Assay (1:100-1:5000)
NoteUsers are strongly advised to determine the optimal dilution of antibody to use for their specific applications.

 

Specifity: The antibody is a rabbit Polyclonal antibody raised against CFTR. It has been selected for its ability to recognize CFTR in immunohistochemical staining and western blotting.

Stability: 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.

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

Notes: For In vitro laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.

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