Western blot analysis of extracts of various cell lines, using Phospho-SMC1-S957 antibody (AP0090) at 1:1000 dilution. HeLa and NIH/3T3 cells were treated by UV for 15-30 minutes.|Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.|Lysates/proteins: 25ug per lane.|Blocking buffer: 3% BSA.|Detection: ECL Basic Kit (RM00020).|Exposure time: 3s.
Immunofluorescence analysis of GFP-RNF168 transgenic U2OS cells using Phospho-SMC1-S957 antibody (AP0090). Green锛欸FP-RNF168 fusion protein expression for DNA damage marker.Blue: DAPI for nuclear staining. RNF168(GFP) can be used to mark cells damaged by UV-A laser for they always gather around DNA damage region.
Western blot analysis of extracts of HeLa cells, using Phospho-SMC1-S957 pAb (AP0090) at 1:1000 dilution or SMC1A antibody (A7008).HeLa cells were treated by UV at room temperature for 15-30 minutes.|Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.|Lysates/proteins: 25ug per lane.|Blocking buffer: 3% BSA.|Detection: ECL Basic Kit (RM00020).|Exposure time: 3s.
Phospho-SMC1-S957 Rabbit pAb
Catalog No:AB-AP0090
Manufacturer:ABclonal
Synonyms:SMC1A;CDLS2;DXS423E;SB1.8;SMC1;SMC1L1;SMC1alpha;SMCB
Applications:WB,IHC,IF,IP
Reactivity:Human,Mouse,Rat
Host:Rabbit
Conjugate:No
€65,00 – €410,00
Product Name: | Phospho-SMC1-S957 Rabbit pAb |
Category: | Phosphorylated Antibodies |
Description: | 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. |
Immunogen: | A synthetic phosphorylated peptide around S957 of human SMC1A (NP_006297.2). |
Gene ID: | 8243 |
Swiss prot: | Q14683 |
Molecular weight: | 143kDa |
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