ELK Bio
CENPS rabbit pAb - ES10529
CENPS rabbit pAb - ES10529
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CENPS rabbit pAb
Sizes: 50μL, 100μL
Catalogue Numbers: ES10529-50, ES10529-100
Citations, Manuals and MSDS Available upon request.
Background: This gene was identified in the neuroblastoma tumor suppressor candidate region on chromosome 1p36. It contains a TFIID-31 domain, similar to that found in TATA box-binding protein-associated factor, TAF (II)31, which is required for p53-mediated transcription activation. This gene was expressed at very low levels in neuroblastoma tumors, and was shown to reduce cell growth in neuroblastoma cells, suggesting that it may have a role in a cell death pathway. The protein is a component of multiple complexes, including the Fanconi anemia (FA) core complex, the APITD1/CENPS complex, and the CENPA-CAD (nucleosome distal) complex. Known functions include an involvement with chromatin associations of the FA core complex, and a role in the stable assembly of the outer kinetochore. Alternative splicing of this gene results in multiple transcript variants. Naturally occurring read-through transcripts also exist
Source: Rabbit
Applications: WB; ELISA
Dilution: WB 1:500-2000 ELISA 1:5000-20000
Reactivity: Human; Rat; Mouse;
Immunogen: Synthesized peptide derived from human protein . at AA range: 70-150
Storage and Stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Observed Band (KD): 15kD
Human Gene ID: 100526739
Human SWISS Prot NO: Q8N2Z9
Subcellular Location: Nucleus. Chromosome, centromere. Chromosome, centromere, kinetochore. Assembly of CENPS and CENPX and its partner subunits CENPT and CENPW at centromeres occurs through a dynamic exchange mechanism. Although exchange is continuous in the cell cycle, de novo assembly starts principally during mid-late S phase and is complete by G2. CENPS is more stably bound at the kinetochore than CENPX (PubMed:19620631, PubMed:24522885). During S phase, rapidly recruited to DNA interstrand cross-links that block replication (PubMed:20347428). Recruited to DNA damage sites about 20 minutes following UV irradiation, reaching a plateau after approximately 40 minutes (PubMed:24522885).
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