Full Product Name
Anti-NBN Antibody
Product Gene Name
anti-NBN antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for O60934
Purity/Purification
Affinity Purification
Concentration
1mg/ml (lot specific)
Immunogen
A synthetic peptide of human NBN
Storage Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Preparation and Storage
Store at -20 degree C. Avoid freeze/thaw cycles.
Other Notes
Small volumes of anti-NBN antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-NBN antibody
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.
Applications Tested/Suitable for anti-NBN antibody
Western Blot (WB)
Application Notes for anti-NBN antibody
WB: 1:500-1:2000
NCBI/Uniprot data below describe general gene information for NBN. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001019859.1
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NCBI GenBank Nucleotide #
NM_001024688.2
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UniProt Primary Accession #
O60934
[Other Products]
UniProt Secondary Accession #
O60672; Q32NF7; Q53FM6; Q63HR6; Q7LDM2; B2R626; B2RNC5[Other Products]
UniProt Related Accession #
O60934[Other Products]
Molecular Weight
84,959 Da
NCBI Official Full Name
nibrin isoform 2
NCBI Official Synonym Full Names
nibrin
NCBI Official Symbol
NBN [Similar Products]
NCBI Official Synonym Symbols
ATV; NBS; P95; NBS1; AT-V1; AT-V2
[Similar Products]
NCBI Protein Information
nibrin
UniProt Protein Name
Nibrin
UniProt Synonym Protein Names
Cell cycle regulatory protein p95; Nijmegen breakage syndrome protein 1
UniProt Gene Name
NBN [Similar Products]
UniProt Synonym Gene Names
NBS; NBS1; P95 [Similar Products]
NCBI Summary for NBN
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. [provided by RefSeq, Jul 2008]
UniProt Comments for NBN
Component of the MRE11-RAD50-NBN (MRN complex) which plays a critical role in the cellular response to DNA damage and the maintenance of chromosome integrity. The complex is involved in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity, cell cycle checkpoint control and meiosis. The complex possesses single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity, which are provided by MRE11. RAD50 may be required to bind DNA ends and hold them in close proximity. NBN modulate the DNA damage signal sensing by recruiting PI3/PI4-kinase family members ATM, ATR, and probably DNA-PKcs to the DNA damage sites and activating their functions. It can also recruit MRE11 and RAD50 to the proximity of DSBs by an interaction with the histone H2AX. NBN also functions in telomere length maintenance by generating the 3' overhang which serves as a primer for telomerase dependent telomere elongation. NBN is a major player in the control of intra-S-phase checkpoint and there is some evidence that NBN is involved in G1 and G2 checkpoints. The roles of NBS1/MRN encompass DNA damage sensor, signal transducer, and effector, which enable cells to maintain DNA integrity and genomic stability. Forms a complex with RBBP8 to link DNA double-strand break sensing to resection. Enhances AKT1 phosphorylation possibly by association with the mTORC2 complex.
Research Articles on NBN
1. The CC genotype of rs2735383 did not confer an increased breast cancer risk, neither in the overall analyses nor in the subgroup analyses.
Precautions
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