RFX5 Polyclonal Antibody | G-AB-11408

RFX5 Polyclonal Antibody | G-AB-11408 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Epigenetics and Nuclear Signaling, Immunology

Synonyms: RFX5

Reactivity: Human

Host: Rabbit

Isotype: IgG

Gene ID: 5993

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human RFX5 (NP_000440.1) .

Clone #:

Conjugation: Unconjugated

Swissprot: P48382

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: IF

Dilution: IF 1:50-1:100

Storage: Store at -20°C. Avoid freeze / thaw cycles.

RFX5 Polyclonal Antibody DataSheet