RFXANK Antibody (4G10)

Product: Entinostat

RFXANK Antibody (4G10) Summary

Immunogen
RFXANK (NP_003712.1, 1 a.a. – 90 a.a.) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. MELTQPAEDLIQTQQTPASELGDPEDPGEEAADGSDTVVLSLFPCTPEPVNPEPDASVSSPQAGSSLKHSTTLTNRQRGNEVSALPATLD
Specificity
RFXANK – regulatory factor X-associated ankyrin-containing protein (4G10)
Isotype
IgG2a Kappa
Clonality
Monoclonal
Host
Mouse
Gene
RFXANK
Purity
IgG purified
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Applications/Dilutions

Dilutions
  • Western Blot
  • ELISA
  • Immunocytochemistry/Immunofluorescence
Application Notes
Antibody reactivity against Recombinant Protein with GST tag on ELISA and WB. GST tag alone is used as a negative control.

Packaging, Storage & Formulations

Storage
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.4)
Preservative
No Preservative
Purity
IgG purified

Notes

Quality control test: Antibody Reactive Against Recombinant Protein.

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for RFXANK Antibody (4G10)

  • ANKRA1Regulatory factor X subunit B
  • ankyrin repeat-containing regulatory factor X-associated protein
  • BLS
  • DNA-binding protein RFXANK
  • F14150_1
  • MGC138628
  • regulatory factor X-associated ankyrin-containing proteinAnkyrin repeat family A protein 1
  • RFXB
  • RFX-BRFX-Bdelta4

Background

Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. This protein contains ankyrin repeats involved in protein-protein interactions. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group B. Two transcript variants encoding different isoforms have been described for this gene, with only one isoform showing activation activity. [provided by RefSeq]

PMID: 27211495