NBN Polyclonal Antibody | G-AB-11817

NBN Polyclonal Antibody | G-AB-11817 | Gentaur Antibodies

Overview: Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation.

Category Type: Polyclonal Antibody

Research Areas: Cancer, Epigenetics and Nuclear Signaling

Synonyms: NBN, AT-V1, AT-V2, ATV, NBS, NBS1, P95, nibrin

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID: 4683

Accession #:

Clonality:

Immunogen: A synthetic peptide of human NBN

Clone #:

Conjugation: Unconjugated

Swissprot: O60934

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: IF

Dilution: IF 1:50-1:200

Storage: Store at -20°C. Avoid freeze / thaw cycles.

NBN Polyclonal Antibody DataSheet