SRCAP Antibody

Code CSB-PA751175XA01HU
Size Enquire
Have Questions? Leave a Message or Start an on-line Chat

Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) SRCAP Polyclonal antibody
Uniprot No.
Target Names
SRCAP
Alternative Names
SRCAP antibody; KIAA0309 antibody; Helicase SRCAP antibody; EC 3.6.4.- antibody; Domino homolog 2 antibody; Snf2-related CBP activator antibody
Raised in
Rabbit
Species Reactivity
Homo sapiens (Human)
Immunogen
Recombinant Homo sapiens (Human) SRCAP protein
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, WB (ensure identification of antigen)
Protocols
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Value-added Deliverables
① 200ug * antigen (positive control);
② 1ml * Pre-immune serum (negative control);
Quality Guarantee
① Antibody purity can be guaranteed above 90% by SDS-PAGE detection;
② ELISA titer can be guaranteed 1: 64,000;
③ WB validation with antigen can be guaranteed positive;
Lead Time
Made-to-order (14-16 weeks)

Customer Reviews and Q&A

 Customer Reviews

There are currently no reviews for this product.

Submit a Review here

Target Background

Function
Catalytic component of the SRCAP complex which mediates the ATP-dependent exchange of histone H2AZ/H2B dimers for nucleosomal H2A/H2B, leading to transcriptional regulation of selected genes by chromatin remodeling. Acts as a coactivator for CREB-mediated transcription, steroid receptor-mediated transcription, and Notch-mediated transcription.
Gene References into Functions
  1. Data show that PCI domain-containing protein 2 (Pcid2) controls lymphoid lineage commitment through the regulation of Snf2-related CREBBP activator protein (SRCAP) remodelling activity. PMID: 29138493
  2. Alterative hypotheses to explain how the Srcap truncating mutations lead to the onset of Floating-Harbor syndrome are presented. PMID: 27208210
  3. Data confirm a mutational hot spot in the final exon of SRCAP in the majority of Floating-Harbor syndrome patients but also show that exon 33 of this gene can be affected. PMID: 25433523
  4. This study implicates the human SRCAP chromatin remodeling complex as a novel regulator of DNA damage responses that orchestrates proper signaling and repair of DSBs in the context of chromatin. PMID: 25176633
  5. Functional studies and reports of patients with additional SRCAP mutations will eventually lead to a better understanding of biological mechanisms underlying this disorder. PMID: 23763483
  6. These results indicate that perturbed skeletal maturation from infancy through adolescence is a characteristic feature in patients with SRCAP mutations. PMID: 24375913
  7. Sequencing of the SRCAP gene demonstrated a de novo mutation matching one of the known FHS-associated mutations. PMID: 23165645
  8. Data indicate that the absence of SRCAP mutations in 3/9 cases suggesting genetic heterogeneity of floating-harbor syndrome (FH syndrome). PMID: 22965468
  9. Our genome-wide expression results demonstrate that SRCAP-mediated H2A.Z deposition at promoter regions is necessary for complete gene reactivation induced by DNA demethylation. PMID: 22479200
  10. Sanger sequencing identified mutations in SRCAP in eight more affected persons. PMID: 22265015
  11. HCV NS3 protein is involved in the activation of the Notch-signaling pathway through the targeting to both SRCAP and p400 PMID: 21673954
  12. These data identify SRCAP as a physiologically relevant mediator of PSA expression, and demonstrate that SRCAP plays a role in prostate cancer cell proliferation. PMID: 20432434
  13. SRCAP functions as a coactivator to regulate transcription initiated by several signaling pathways. PMID: 14500758
  14. SRCAP is implicated in developmental gene activation PMID: 16024792
  15. SRCAP-containing complex supports ATP-dependent exchange of histone dimers containing H2B and H2A.Z into mononucleosomes reconstituted with recombinant H2A, H2B, H3, and H4. PMID: 16634648
  16. Methods for purification and assay of the SRCAP chromatin remodeling complexes are described. PMID: 17101442
  17. SRCAP is recruited to promoters and is critical for the deposition of H2A.Z. PMID: 17617668

Show More

Hide All

Involvement in disease
Floating-Harbor syndrome (FLHS)
Subcellular Location
Nucleus.
Protein Families
SNF2/RAD54 helicase family, SWR1 subfamily
Database Links

HGNC: 16974

OMIM: 136140

KEGG: hsa:10847

STRING: 9606.ENSP00000262518

UniGene: Hs.620916

icon of phone
Call us
301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
icon of address
Address
7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
icon of social media
Join us with

Subscribe newsletter

Leave a message

* To protect against spam, please pass the CAPTCHA test below.
CAPTCHA verification
© 2007-2024 CUSABIO TECHNOLOGY LLC All rights reserved. 鄂ICP备15011166号-1