SCC2 Antibody

Code CSB-PA823952XA01SVG
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Product Details

Full Product Name
Rabbit anti-Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) SCC2 Polyclonal antibody
Uniprot No.
Target Names
SCC2
Alternative Names
SCC2 antibody; YDR180W antibody; YD9395.14 antibody; Sister chromatid cohesion protein 2 antibody
Raised in
Rabbit
Species Reactivity
Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast)
Immunogen
Recombinant Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) SCC2 protein
Immunogen Species
Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast)
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)
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Plays a structural role in chromatin and is involved in sister chromatid cohesion. Forms a complex with SCC4 required for the stable association of the cohesin complex with chromatin, which may act by hydrolyzing ATP from SMC1 and SMC3 heads. Binds to the nucleosome-free promoter regions of ribosomal protein genes and tRNA genes. Involved in transcriptional regulation by cooperating with the RSC complex to maintain nucleosome exhaustion at its binding sites.
Gene References into Functions
  1. Nipbl seems to have also additional roles, for instance as transcription factor.This chapter summarizes our current knowledge on kollerin function and the recent studies on the genomic localization of Scc2, highlighting and critically discussing controversial data. PMID: 27797076
  2. The role of Scc2 in cohesin loading PMID: 27280786
  3. Authors conclude that normal Scc2 function requires modulation of its phosphorylation state and suggest that scc2 phosphomimetic mutants cause an increased incidence of abortive cohesin deposition events that result in compromised cohesin complex integrity and Mcd1 turnover. PMID: 26354421
  4. Scc2 normally promotes a gene expression program that supports translational fidelity. . translational dysfunction may contribute to the human disorder Cornelia de Lange syndrome, which is caused by mutations in NIPBL, the human ortholog of SCC2. PMID: 26176819
  5. These findings reveal the role of Scc4 in determining the localization of cohesin loading and establish a molecular basis for Scc2/4 recruitment to centromeres. PMID: 26038942
  6. After in activation of Scc2, DNA damage specific transcriptional response is distorted. PMID: 25483075
  7. Data indicate that Scc2-Scc4 binding sites were strikingly enriched at transcriptional start sites (TSSs). PMID: 25173104
  8. These observations suggest a previously unidentified mechanism for the spatiotemporal regulation of cohesin association with chromosomes through cell cycle regulation of Scc2 cohesin deposition activity by Scc2 dephosphorylation and cleavage. PMID: 24778232
  9. SMC proteins and Scc2 localize to the silenced domain, and Scc2 binding requires the presence of gamma-H2A. PMID: 23733345
  10. Scc2 is required for activating the expression of REC8 and Scc2 is necessary for recruiting meiotic cohesin to the chromosome to generate sister-chromatid cohesion. PMID: 21508318
  11. Scc2/Scc4 resides at previously mapped cohesin-associated regions (CARs) in pericentromeric and arm regions, and that Scc2/Scc4-cohesin colocalization persists after the initial deposition of cohesins in G1/S phase PMID: 19797771
  12. Mutations in Scc2 may affect the loading or dynamics of cohesin, condensin, or both. PMID: 19948494

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Subcellular Location
Nucleus. Chromosome, centromere.
Protein Families
SCC2/Nipped-B family
Database Links

KEGG: sce:YDR180W

STRING: 4932.YDR180W

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