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SMC1A Recombinant Rabbit mAb

Cat No.: RMA02812
规格:
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  • Western blot analysis of Anti-SMC1A antibody(RMA02812) Gel: 6%SDS-PAGE Lysate: 20 μg Primary antibody: RMA02812(SMC1A antibody)at dilution 1:1000 Secondary antibody: Goat anti rabbit IgG (SPA10002)at 1:1000 dilution

Product Name: SMC1A Recombinant Rabbit mAb
Cat No.: RMA02812
Clonality: Monoclonal
Species Reactivity: Human, Mouse, Rat
Tested Applications: WB, IHC, IP
Recommended Dilution: WB, IHC, IP
Size: 30ul 50ul 100uL
Format: Liquid
Source: Rabbit
Purification Method: Affinity Purification
Isotype: IgG
Conjugate: Un-conjugated
Storage: Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a
Immunogen: A synthetic peptide of human SMC1
Calculated Molecular Weight: 143 kDa
Observed Molecular Weight: 145 kDa
GenBank Accession Number: Q14683
Gene ID (NCBI): 8243
Synonyms: SMC1; SMCB; CDLS2; SB1.8; SMC1L1; DXS423E; SMC1alpha
Background: Proper cohesion of sister chromatids is a prerequisite for the correct segregation of chromosomes during cell division. The cohesin multiprotein complex is required for sister chromatid cohesion. This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins, SMC3 and either SMC1B or the protein encoded by this gene. Most of the cohesin complexes dissociate from the chromosomes before mitosis, although those complexes at the kinetochore remain. Therefore, the encoded protein is thought to be an important part of functional kinetochores. In addition, this protein interacts with BRCA1 and is phosphorylated by ATM, indicating a potential role for this protein in DNA repair. This gene, which belongs to the SMC gene family, is located in an area of the X-chromosome that escapes X inactivation. Mutations in this gene result in Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Category: Primary Ab
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