KO Validated Antibodies 1
Anti-NBN Antibody (CAB0783)[KO Validated]
- SKU:
- CAB0783
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Cycle
Description
Antibody Name: | Anti-NBN Antibody [KO Validated] |
Antibody SKU: | CAB0783 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IHC |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 435-754 of human NBN (NP_002476.2). |
Application: | WB IHC |
Recommended Dilution: | WB 1:500 - 1:1000 IHC 1:50 - 1:100 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | 293T, Mouse testis, Rat testis |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 435-754 of human NBN (NP_002476.2). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | KLPS INKS KDRA SQQQ QTNS IRNY FQPS TKKR ERDE ENQE MSSC KSAR IETS CSLL EQTQ PATP SLWK NKEQ HLSE NEPV DTNS DNNL FTDT DLKS IVKN SASK SHAA EKLR SNKK REMD DVAI EDEV LEQL FKDT KPEL EIDV KVQK QEED VNVR KRPR MDIE TNDT FSDE AVPE SSKI SQEN EIGK KREL KEDS LWSA KEIS NNDK LQDD SEML PKKL LLTE FRSL VIKN STSR NPSG INDD YGQL KNFK KFKK VTYP GAGK LPHI IGGS DLIA HHAR KNTE LEEW LRQE MEVQ NQHA KEES LADD LFRY NPYL KRRR |
Gene ID: | 4683 |
Uniprot: | O60934 |
Cellular Location: | Chromosome, Nucleus, PML body, telomere |
Calculated MW: | 84kDa |
Observed MW: | 95kDa/70kDa |
Synonyms: | NBN, AT-V1, AT-V2, ATV, NBS, NBS1, P95, nibrin |
Background: | 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. |
UniProt Protein Function: | NBS1: a member of the MRE11/RAD50 double-strand break repair complex. Involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. Mutation results in the Nijmegen breakage syndrome (NBS), an autosomal recessive chromosomal instability syndrome. |
UniProt Protein Details: | Protein type:Cell cycle regulation; DNA repair, damage Chromosomal Location of Human Ortholog: 8q21 Cellular Component: cytosol; Mre11 complex; nuclear chromosome, telomeric region; nuclear inclusion body; nucleolus; nucleoplasm; nucleus; PML body; replication fork Molecular Function:ATP-dependent DNA helicase activity; damaged DNA binding; protein binding; protein N-terminus binding; transcription factor binding Biological Process: blastocyst growth; cell cycle arrest; cell proliferation; DNA damage checkpoint; DNA damage response, signal transduction by p53 class mediator; DNA duplex unwinding; DNA repair; double-strand break repair; double-strand break repair via homologous recombination; double-strand break repair via nonhomologous end joining; double-strand break repair via synthesis-dependent strand annealing; isotype switching; meiotic cell cycle; mitotic cell cycle checkpoint; mitotic cell cycle G2/M transition DNA damage checkpoint; neuromuscular process controlling balance; positive regulation of kinase activity; positive regulation of protein amino acid autophosphorylation; positive regulation of telomere maintenance; regulation of DNA replication initiation; telomere maintenance; telomeric 3' overhang formation Disease: Aplastic Anemia; Leukemia, Acute Lymphoblastic; Nijmegen Breakage Syndrome |
NCBI Summary: | 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 Code: | O60934 |
NCBI GenInfo Identifier: | 74762960 |
NCBI Gene ID: | 4683 |
NCBI Accession: | O60934.1 |
UniProt Secondary Accession: | O60934,O60672, Q32NF7, Q53FM6, Q63HR6, Q7LDM2, B2R626 B2RNC5, |
UniProt Related Accession: | O60934 |
Molecular Weight: | 84,959 Da |
NCBI Full Name: | Nibrin |
NCBI Synonym Full Names: | nibrin |
NCBI Official Symbol: | NBN |
NCBI Official Synonym Symbols: | ATV; NBS; P95; NBS1; AT-V1; AT-V2 |
NCBI Protein Information: | nibrin |
UniProt Protein Name: | Nibrin |
UniProt Synonym Protein Names: | Cell cycle regulatory protein p95; Nijmegen breakage syndrome protein 1 |
Protein Family: | Nibrin |
UniProt Gene Name: | NBN |
UniProt Entry Name: | NBN_HUMAN |