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Anti-RFX5 Rabbit Polyclonal Antibody
Anti-RFX5 Rabbit Polyclonal Antibody
Catalog #: 10106-942
Supplier:  Prosci
RFX5 antibody
Anti-RFX5 Rabbit Polyclonal Antibody
Catalog #: 10106-942
Supplier:  Prosci
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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    regulatory factor X, 5 (influences HLA class II expression)
  • Clonality:
    Polyclonal
  • Gene ID:
    P48382
  • Host:
    Rabbit
  • Reactivity:
    Human
  • Antigen symbol:
    RFX5
  • Conjugation:
    Unconjugated
  • ELISA:
    Yes
  • Size:
    100 ul
  • Western blot:
    Yes
  • Form:
    Liquid
  • Antigen synonyms:
    RFX5
  • Storage buffer:
    Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
  • Molecular weight:
    68 kDa, 65 kDa
  • Storage temperature:
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store RFX5 antibody at –20 °C. As with any antibody avoid repeat freeze-thaw cycles.
  • Shipping temperature:
    4 °C
  • Immunogen:
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human RFX5.
  • Purification:
    Antibody is purified by protein A chromatography method.
  • Cat. no.:
    10106-942
  • Supplier No.:
    28-765

Specifications

About this item

RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. RFX is a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX.A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX.A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX, a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al., 1995). RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. Multiple alternatively spliced transcript variants have been found but the full-length natures of only two have been determined.

RFX5 antibody can be used for detection of RFX5 by ELISA at 1:1562500. RFX5 antibody can be used for detection of RFX5 by western blot at 2.5 ?g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Antibody is purified by protein A chromatography method.

Antibody is lyophilized in PBS buffer with 2% sucrose. Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Type: Primary
Antigen: RFX5
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype:
Reactivity: Human

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