NBN / NBS1 Recombinant monoclonal antibody 82884-1-RR proteintech

$149.00
In stock
SKU
82884-1-RR
Catalog No.SizePrice (USD)
82884-1-RR-20UL20 μL$149.00
82884-1-RR-100UL100 μL$449.00
82884-1-RR-10X100UL1 mL (10 x 100 μL vials)$3,592.00
Catalog Number82884-1-RR
SynonymsNBN, 1C16, AT V1, AT V2, ATV
HostRabbit
Reactivityhuman
FormLiquid
FormulationPBS, Azide, Glycerol
ApplicationsWB, ELISA
Host / IsotypeRabbit / IgG
Tested Applications — Positive WB detected inJurkat cells, HeLa cells, A549 cells, A431 cells,
Recommended Dilutions — Western Blot (WB)WB : 1:2000-1:10200
Positive WB detected inJurkat cells, HeLa cells, A549 cells, A431 cells,
Western Blot (WB)WB : 1:2000-1:10200
Tested Reactivityhuman
ClassRecombinant
TypeAntibody
ImmunogenPeptide Predict reactive species
Full Namenibrin
Calculated Molecular Weight85 kDa
Observed Molecular Weight90-95 kDa
GenBank Accession NumberBC136803
Gene SymbolNBN
Gene ID (NCBI)4683
RRIDAB_3670602
ConjugateUnconjugated
Purification MethodProtein A purification
UNIPROT IDO60934
Storage BufferPBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20 o C storage. 20ul sizes contain 0.1% BSA.
WB protocol for NBN / NBS1 antibody 82884-1-RRDownload protocol
Citations-
DilutionsWB : 1:2000-1:10200
IsotypeIgG
ClonalityRecombinant
Clone Number1C16
ConjugationUnconjugated

NBN, also named as NBS, NBS1, and P95, is a 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 MRE11A. NBN modulates 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. 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 checkpoints and there is some evidence that NBN is involved in G1 and G2 checkpoints. Defects in NBN are the cause of Nijmegen breakage syndrome (NBS). Defects in NBN are a cause of genetic susceptibility to breast cancer (BC). Defects in NBN may be associated with aplastic anemia. Defects in NBN might play a role in the pathogenesis of childhood acute lymphoblastic leukemia (ALL). The antibody is specific to NBN. The full-length NBN protein, with an apparent molecular weight of 95 kDa and the two protein fragments of 26 and 70 kDa arising from the c.657_661del5 (p.K219fsX19) mutation, and the 80 kDa protein found in patient RR with the mutation c.742_743insGG leading to excision of exons 6 and 7 from the NBN mRNA are shown. (PMID: 26265251) The predicted molecular weight of NBN protein (p95) is 85kDa, and actually detection result is about 95kDa(PMID: 23762398). Protocols Product Specific Protocols WB protocol for NBN / NBS1 antibody 82884-1-RR Download protocol Standard Protocols Click here to view our Standard Protocols

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