Mouse Anti-NEK2 Recombinant Antibody (2A10) (CBMAB-N1924-WJ)
Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
NEK2-mediated phosphorylation of CEP68 promotes CEP68 dissociation from the centrosome and its degradation at the onset of mitosis (PubMed:25704143).
Involved in the regulation of centrosome disjunction (PubMed:26220856).
Isoform 1:
Phosphorylates and activates NEK11 in G1/S-arrested cells.
Isoform 2:
Not present in the nucleolus and, in contrast to isoform 1, does not phosphorylate and activate NEK11 in G1/S-arrested cells.
Cell division Source: UniProtKB-KW
Centrosome separation Source: UniProtKB
Chromosome segregation Source: UniProtKB
Meiotic cell cycle Source: UniProtKB-KW
Mitotic cell cycle Source: ProtInc
Mitotic sister chromatid segregation Source: Ensembl
Mitotic spindle assembly Source: Ensembl
Negative regulation of centriole-centriole cohesion Source: UniProtKB
Negative regulation of DNA binding Source: Ensembl
Positive regulation of telomerase activity Source: BHF-UCL
Positive regulation of telomere capping Source: BHF-UCL
Positive regulation of telomere maintenance via telomerase Source: BHF-UCL
Protein autophosphorylation Source: UniProtKB
Protein phosphorylation Source: UniProtKB
Regulation of attachment of spindle microtubules to kinetochore Source: UniProtKB
Regulation of mitotic centrosome separation Source: UniProtKB
Regulation of mitotic nuclear division Source: ProtInc
Spindle assembly Source: UniProtKB
Nucleus
nucleolus
Cytoplasm
Cytoskeleton
centrosome
spindle pole
Other locations
kinetochore
centromere
Note: STK3/MST2 and SAV1 are required for its targeting to the centrosome. Colocalizes with SGO1 and MAD1L1 at the kinetochore. Not associated with kinetochore in the interphase but becomes associated with it upon the breakdown of the nuclear envelope. Has a nucleolar targeting/ retention activity via a coiled-coil domain at the C-terminal end.
Isoform 2:
Cytoplasm
Note: Predominantly cytoplasmic.
Isoform 4:
Nucleus
Cytoskeleton
centrosome
Note: Predominantly nuclear.
A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols
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