Product Name
RFXAP, Blocking Peptide
Full Product Name
RFXAP Peptide - middle region
Product Gene Name
RFXAP blocking peptide
[Similar Products]
RFXAP peptide (MBS3226418) is used for blocking the activity of RFXAP antibody (MBS3201396)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for O00287
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of RFXAP blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
RFXAP blocking peptide
This is a synthetic peptide designed for use in combination with anti-RFXAP antibody made
Target Description: RFXAP is part of the RFX complex that binds to the X-box of MHC II promoters.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 ankyrin-containing 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. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group D. Transcript variants utilizing different polyA signals have been found for this gene. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because transcript sequence consistent with the reference genome assembly was not available for all regions of the RefSeq transcript. The extent of this transcript is supported by transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Product Categories/Family for RFXAP blocking peptide
Peptide
Applications Tested/Suitable for RFXAP blocking peptide
Western Blot (WB)
NCBI/Uniprot data below describe general gene information for RFXAP. It may not necessarily be applicable to this product.
NCBI Accession #
NP_000529
[Other Products]
NCBI GenBank Nucleotide #
NM_000538
[Other Products]
UniProt Primary Accession #
O00287
[Other Products]
UniProt Related Accession #
O00287[Other Products]
NCBI Official Full Name
regulatory factor X-associated protein
NCBI Official Synonym Full Names
regulatory factor X associated protein
NCBI Official Symbol
RFXAP [Similar Products]
NCBI Protein Information
regulatory factor X-associated protein
UniProt Protein Name
Regulatory factor X-associated protein
UniProt Synonym Protein Names
RFX DNA-binding complex 36 kDa subunit
Protein Family
Regulatory factor X-associated protein
UniProt Gene Name
RFXAP [Similar Products]
UniProt Entry Name
RFXAP_HUMAN
NCBI Summary for RFXAP
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 ankyrin-containing 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. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group D. Transcript variants utilizing different polyA signals have been found for this gene. [provided by RefSeq, Jul 2008]
UniProt Comments for RFXAP
RFXAP: Part of the RFX complex that binds to the X-box of MHC II promoters. Defects in RFXAP are a cause of bare lymphocyte syndrome type 2 (BLS2); 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.
Protein type: DNA-binding
Chromosomal Location of Human Ortholog: 13q14
Cellular Component: nucleus
Molecular Function: DNA binding; transcription coactivator activity; transcription factor activity
Biological Process: positive regulation of transcription, DNA-dependent
Disease: Bare Lymphocyte Syndrome, Type Ii
Research Articles on RFXAP
1. Data show a negative correlation between microRNA miR-212-3p and regulatory factor X-associated protein (RFXAP) in pancreatic cancer (PC) tissue.
Precautions
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Disclaimer
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