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NBS1 Mouse, Unlabeled, Clone: 34, BD

Mouse Monoclonal Antibody

Supplier:  BD Biosciences 611870

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Catalog No. BDB611870

Item Discontinued This item has been discontinued by Fisher Scientific. Please to view product availability in your area.


Description

Description

Nijmegen Breakage Syndrome (NBS) is characterized by extreme radiation sensitivity and chromosomal instability. The NBS1 gene product, p95/nibrin/NBS1, forms a complex with Rad50 and Mre11. Cells deficient in this complex have problems with DNA double-strand break repair, cell cycle checkpoint control, and telomere length maintenance. NBS1 contains a forkhead-associated domain (FHA) and a breast cancer carboxy-terminal domain (BRCT) in the N-terminal region. Both of these domains have been found in DNA-damage responsive cell cycle checkpoint proteins. The complex containing NBS1, Rad50, and Mre11 possesses manganese-dependent single stranded DNA endonuclease and 3′ to 5′ exonuclease activities. In addition, NBS1 is required for DNA-damage dependent phosphorylation of Mre11. This phosphorylation may be required for proper nuclear localization of the NBS1-Rad50-Mre11 complex to sites of DNA double-strand breaks. NBS1 interacts directly with telomere repeat binding factor, TRF1, via its C-terminal region, and both NBS1 and Mre11 co-localize with TRF1 at promyelocytic leukemia nuclear bodies. Thus, the NBS1-Rad50-Mre11 complex may be important for both DNA damage repair, and telomere length maintenance.

Host Species: Mouse
Clone: 34
Isotype: IgG1
Species Reactivity [for Features Main]: Human
Immunogen: Human NBS1 aa. 620-732

Immunofluorescence, Western Blotting

TRUSTED_SUSTAINABILITY
Specifications

Specifications

NBS1
Monoclonal
250μg/mL
Nijmegen Breakage Syndrome-1
Mouse
Affinity Purified
RUO
Primary
Store undiluted at -20°C.
Western Blot
34
Unconjugated
Aqueous buffered solution containing BSA, glycerol, and ≤0.09% sodium azide.
Human NBS1 aa. 620-732
50 μg
Cell Biology
Canine, Chicken, Human, Mouse, Rat
IgG1
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