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VRK1 Antibody (Center)(Ascites)

Mouse Monoclonal Antibody (Mab)

     
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  • 1 - VRK1 Antibody (Center)(Ascites) AM2226a
    VRK1 Antibody (Center)(Cat. #AM2226a) western blot analysis in Hela,HL-60 cell line lysates (35μg/lane).This demonstrates the VRK1 antibody detected the VRK1 protein (arrow).
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, E
Primary Accession Q99986
Reactivity Human
Host Mouse
Clonality Monoclonal
Isotype IgG1
Clone Names 1015CT2.1.1
Calculated MW 45476 Da
Additional Information
Gene ID 7443
Other Names Serine/threonine-protein kinase VRK1, Vaccinia-related kinase 1, VRK1
Target/Specificity Purified His-tagged VRK1 protein was used to produced this monoclonal antibody.
Dilution WB~~1:5000
E~~Use at an assay dependent concentration.
Format Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsVRK1 Antibody (Center)(Ascites) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name VRK1 {ECO:0000303|PubMed:9344656, ECO:0000312|HGNC:HGNC:12718}
Function Serine/threonine kinase involved in the regulation of key cellular processes including the cell cycle, nuclear condensation, transcription regulation, and DNA damage response (PubMed:14645249, PubMed:18617507, PubMed:19103756, PubMed:33076429). Controls chromatin organization and remodeling by mediating phosphorylation of histone H3 on 'Thr-4' and histone H2AX (H2aXT4ph) (PubMed:31527692, PubMed:37179361). It also phosphorylates KAT5 in response to DNA damage, promoting KAT5 association with chromatin and histone acetyltransferase activity (PubMed:33076429). Is involved in the regulation of cell cycle progression of neural progenitors, and is required for proper cortical neuronal migration (By similarity). Is involved in neurite elongation and branching in motor neurons, and has an essential role in Cajal bodies assembly, acting through COIL phosphorylation and the control of coilin degradation (PubMed:21920476, PubMed:31090908, PubMed:31527692). Involved in Golgi disassembly during the cell cycle: following phosphorylation by PLK3 during mitosis, it is required to induce Golgi fragmentation (PubMed:19103756). Phosphorylates BANF1: disrupts its ability to bind DNA, reduces its binding to LEM domain-containing proteins and causes its relocalization from the nucleus to the cytoplasm (PubMed:16495336). Phosphorylates TP53BP1 and p53/TP53 on 'Thr-18', preventing the interaction between p53/TP53 and MDM2 (PubMed:10951572, PubMed:31527692). Phosphorylates ATF2 which activates its transcriptional activity (PubMed:15105425). Phosphorylates JUN (PubMed:31527692).
Cellular Location Nucleus. Cytoplasm. Nucleus, Cajal body. Note=Enriched on chromatin during mitosis.
Tissue Location Widely expressed. Highly expressed in fetal liver, testis and thymus.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

BACKGROUND

Serine/threonine kinase involved in Golgi disassembly during the cell cycle: following phosphorylation by PLK3 during mitosis, required to induce Golgi fragmentation. Acts by mediating phosphorylation of downstream target protein. Phosphorylates 'Thr-18' of p53/TP53 and may thereby prevent the interaction between p53/TP53 and MDM2. Phosphorylates casein and histone H3. Phosphorylates BANF1: disrupts its ability to bind DNA, reduces its binding to LEM domain-containing proteins and causes its relocalization from the nucleus to the cytoplasm.

REFERENCES

Nezu J., et al. Genomics 45:327-331(1997).
Lopez-Borges S., et al. Oncogene 19:3656-3664(2000).
Barcia R., et al. Arch. Biochem. Biophys. 399:1-5(2002).
Nichols R.J., et al. J. Biol. Chem. 279:7934-7946(2004).
Blanco S., et al. FEBS J. 273:2487-2504(2006).

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