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RFX5 rabbit pAb

Refer to | for labeled antibodies

Specification

BYab-11687

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Product introduction Experimental scheme Citation Related products

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Host
Reactiveness
Use
Molecular weight (DA)
Immunogen
Synthesized peptide derived from human RFX5 AA range: 491-541
Specificity
This antibody detects endogenous levels of RFX5 at Human/Mouse
Source
Polyclonal, Rabbit,IgG
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Dilution rate
WB 1:500-2000;IHC-p 1:50-300
Purification process (Immunogen)
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration
1 mg/ml
Background
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. [provided by RefSeq, Jul 2008],
Function
disease:Defects in RFX5 are a cause of bare lymphocyte syndrome type 2 (BLS2) [MIM:209920]; also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency. BLS2 is a severe combined immunodeficiency disease with early onset. It is characterized by a profound defect in constitutive and interferon-gamma induced MHC II expression, absence of cellular and humoral T-cell response to antigen challenge, hypogammaglobulinemia and impaired antibody production. The consequence include extreme susceptibility to viral, bacterial and fungal infections.,domain:The N-terminus is required for its association with RFXANK and RFXAP, for assembly of the RFX complex, and for binding of this complex to its X box target site in the MHC-II promoter. The C-terminus mediates cooperative binding between the RFX complex and NF-Y.,function:Activates transcription from class II
Gene Name
RFX5
Protein name
RFX5
Abbreviation
RFX5
Other name
Fields
>>Antigen processing and presentation;>>Tuberculosis;>>Primary immunodeficiency
Human gene ID
5993
Human protein sequence Database
P48382
Mouse gene ID
53970
Mouse protein sequence database
Q9JL61
Rat gene ID
Rat protein sequence database
Cellular localization
Nucleus.
Tissue expression
Ubiquitous.
Storage
-20°C/1 year

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RFX5 rabbit pAb

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