SMC1A Recombinant Rabbit mAb
Cat No.: ARM2811
Size:
Product Name: | SMC1A Recombinant Rabbit mAb |
Cat No.: | ARM2811 |
source: | Rabbit |
reactivity: | Human, Mouse, Rat |
applications: | WB, IHC, IP |
clonality: | Monoclonal |
recommended dilution: | WB, IHC, IP |
format: | Liquid |
isotype: | IgG |
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 |
purification method: | Affinity Purification |
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 and 0.05% BSA. Stable for 12 months from date of receipt. |
synonyms: | SMC1; SMCB; CDLS2; SB1.8; SMC1L1; DXS423E; SMC1alpha |
category: | Primary Ab |
concentration: | 1mg/ml |
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] |