NBS1/NBN Rabbit pAb (APR27621N) APR27621N
Specifications
| 50µl / 100µl / 200µl |
Product info:
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.
Alternative names:
NBN; AT-V1; AT-V2; ATV; NBS; NBS1; P95; nibrin
Species reactivity:
Human, Mouse, Rat
Host:
Rabbit
Cellular localisation:
Chromosome, Nucleus, PML body, telomere
Isotype:
IgG
Immunogen:
A synthetic peptide of human NBS1/NBS1/NBN
Positive control:
Jurkat, HeLa, MCF7, Mouse heart, Rat kidney
AA Sequence:
Email info@sobekbio.com for sequence
Purification:
Affinity purification
Molecular weight:
Calculated MW: 84kDa Observed MW: 100kDa
Form:
Liquid
Applications:
WB (Homo sapiens) IF (Homo sapiens)
Dilution:
WB 1:500 - 1:2000 IF 1:50 - 1:200
Storage buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
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.
More info:
Email: info@sobekbio.com
Orders:
Email: orders@sobekbio.com
