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Phospho-SMC1A-S957 pAb

Catalog # Availability Size / Price Inquiry
AMR00840N-1 50ul / $395
AMR00840N-2 100ul / $495
AMR00840N-3 200ul / $595

Phospho-SMC1A-S957 pAb

Brand

Leading Biology

Catalog Number

AMR00840N

Product Type

Phosphorylated Antibodies

Field of Research

Cell Biology & Developmental Biology>Apoptosis

Product Overview

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality Phospho-SMC1A-S957 pAb.

Molecular Weight

Calculated MW: 143kDa Observed MW: 160kDa

Species Reactivity

Rabbit

Immunogen

A synthetic phosphorylated peptide around S957 of human SMC1A (NP_006297.2).

Cross Reactivity

Human,Mouse,Rat

Isotype

IgG

GeneID

UniProt ID

Purity

Affinity purification

Storage & Stability

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

Storage Buffer

Buffer: PBS with 50% glycerol, pH7.3.

Applications

WB,IHC,IF,IP

Dilution

WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:20 - 1:100

Product 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.

Synonyms

SMC1A; CDLS2; DXS423E; SB1.8; SMC1; SMC1L1; SMC1alpha; SMCB; structural maintenance of chromosomes 1A

Images

Western blot analysis of extracts of various cell lines, using Phospho-SMC1A-S957 antibody.

Immunofluorescence analysis of U2OS cells using Phospho-SMC1A-S957 antibody.

Immunofluorescence analysis of GFP-RNF168 transgenic U2OS cells using Phospho-SMC1A-S957 antibody.

Specification

Quantity

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