Product Category: | Human lentivirus expressing RFX5 |
Description: | Premade lentivirus for over-expression of human RFX5 and control, ready to use format. |
Gene Name: | regulatory factor X5 |
Gene Symbol: | RFX5 |
Synonyms: | MHC2D3; MHC2D5 |
ACCN: | NM_000449.4 |
Gene ID: | 5993 |
Vector: | PDS279_pL-CMV-GFP-ccdB-puro |
Promoter: | CMV |
Selection Antibiotic: | Puromycin |
Titer: | ≥1E+8TU/ml |
Buffer: | PBS |
Storage: | -80°C |
Documents: | Manual-Ready-to-Use Recombinant Lentivirus |
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.
Optional Services
Name | Catalog # | Turnaround Time | View |
Gene Synthesis | S0012 | Quote | ![]() |
Lentivirus Packaging | S0032 | Quote | ![]() |
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