N3037

Anti-NBS1 (Nibrin), C-terminal antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

• Numero MDL: MFCD07784852
• Codice UNSPSC: 12352203
• NACRES: NA.41

Proprietà

• Origine biologica: rabbit
• Coniugato: unconjugated
• Forma dell’anticorpo: affinity isolated antibody
• Tipo di anticorpo: primary antibodies
• Clone: polyclonal
• Stato: buffered aqueous solution
• PM: antigen 95 kDa
• Reattività contro le specie: human
• tecniche: immunoprecipitation (IP): 2-4 μg using HeLa cell lysates; indirect immunofluorescence: 5-10 μg/mL; microarray: suitable; western blot: 0.25-0.5 μg/mL using extracts of 293T cells transfected with recombinant NBS1; western blot: 0.5-1 μg/mL using MCF7 nuclear extracts
• N° accesso UniProt: O60934
• Condizioni di spedizione: dry ice
• Temperatura di conservazione: −20°C
• modifica post-traduzionali bersaglio: unmodified
• Informazioni sul gene: human ... NBN(4683) ; mouse ... Nbn(27354) ; rat ... Nbn(85482)

Descrizione

Descrizione generale

Nibrin (NBS1) is made up of 754 amino acids.

Nibrin is encoded by the gene mapped to human chromosome 8q21.3. The protein has two domains found in the cell cycle checkpoint proteins, forkhead-associated domain (FHA), and an adjacent breast cancer carboxy-terminal domain (BRCT).

Immunogeno

synthetic peptide corresponding to amino acids 735-753 of human NBS1 (nibrin), conjugated to KLH via an N-terminal added cysteine residue. The immunizing peptide differs from the rat and mouse corresponding sequences in two amino acids.

Applicazioni

Anti-NBS1 (Nibrin), C-terminal antibody produced in rabbit has been used in:

• immunoblotting
• immunofluorescence
• immunoprecipitation

Azioni biochim/fisiol

Nibrin (NBS1) is involved in stabilizing genomes and has a role in development of cancers. It also takes part in the repair mechanism after double strand breaks in the DNA. Mutations in the gene encoding NBS1 have been associated with Nijmegen breakage syndrome (NBS).

Nibrin (NBS1) 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)/RAD50 ionizing radiation-induced foci, revealing a molecular link between double-strand break (DSB) repair 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, NBS1 is phosphorylated in Ser343 in an ataxia-telangiectasia mutated ATM-dependent manner.

Stato fisico

Solution in 0.01 M phosphate buffered saline containing 15 mM sodium azide.

Esclusione di responsabilità

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.