N9287

Monoclonal Anti-NBS1 (Nibrin) antibody produced in mouse

~2 mg/mL, clone NBS1-501, purified immunoglobulin, buffered aqueous solution

• Sinônimo(s): Anti-Nijmegen Breakage Syndrome, Anti-p95 Protein of NBS1.MRE11/RAD50 Complex
• Número MDL: MFCD03455620
• Código UNSPSC: 12352203
• NACRES: NA.41

Propriedades

• fonte biológica: mouse
• conjugado: unconjugated
• forma do anticorpo: purified immunoglobulin
• tipo de produto de anticorpo: primary antibodies
• clone: NBS1-501, monoclonal
• forma: buffered aqueous solution
• peso molecular: antigen ~95 kDa
• reatividade de espécies: human
• concentração: ~2 mg/mL
• técnica(s): immunocytochemistry: suitable; immunoprecipitation (IP): suitable; microarray: suitable; western blot: 2-4 μg/mL using nuclear extract of HEK 293T expressing recombinant human NBS1
• Isotipo: IgG1
• nº de adesão UniProt: O60934
• Condições de expedição: dry ice
• temperatura de armazenamento: −20°C
• modificação pós-traducional do alvo: unmodified
• Informações sobre genes: human ... NBN(4683)

Descrição

Descrição geral

Monoclonal Anti-NBS1 (Nibrin) (mouse IgG1isotype) is derived from the hybridoma NBS1-501 produced by the fusion of mouse myeloma cells (NS1 cells) and splenocytes from BALB/c mice immunized with a synthetic peptide of human NBS1. Nibrin is mapped to human chromosome 8q21.3. The encoded protein has two domains found in the cell cycle checkpoint proteins, forkhead-associated domain (FHA), and an adjacent breast cancer carboxy-terminal domain (BRCT).

Imunogênio

synthetic peptide corresponding to amino acids 206-220 of human NBS1.

Aplicação

Monoclonal Anti-NBS1 (Nibrin) antibody produced in mouse has been used in:

• antibody microarray
• immunocytochemistry
• immunoblotting
• immunoprecipitation
• enzyme linked immunosorbent assay (ELISA)

Ações bioquímicas/fisiológicas

NBS1(Nibrin) was first isolated as a protein involved in DNA repair through analysis of mutations in patients with this syndrome. p95/NBS1(Nibrin) deficiency abrogates the formation of the Meiotic recombination 11 homolog 1(MRE11) / DNA repair protein RAD50 ionizing radiation-induced foci, revealing a molecular link between double-stranded break repair (DSB) and cell cycle checkpoint functions. The phenotypic similarities between ataxia-telangiectasia (AT) and Nijmegen breakage syndrome had suggested that ataxia-telangiectasia mutated gene (ATM) and NBS1 functions in a common signaling pathway. This was confirmed by the finding that in response to ionizing radiation, NBS1is phosphorylated in Ser343 in an ataxia-telangiectasia mutated ATM-dependent manner.

forma física

Solution in 0.01 M phosphate buffered saline, pH 7.4, and 15 mM sodium azide.

Exoneração de responsabilidade

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Informações de segurança

• Código de classe de armazenamento: 10 - Combustible liquids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable