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Antibodies
Anti-PLK4 Antibody
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产品名称:
Anti-PLK4 Antibody
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简单介绍
Anti-PLK4
Antibody
Anti-PLK4 Antibody
的详细介绍
Overview
Name:
Anti-PLK4
Antibody
See all PLK4 primary antibodies
Description:
Goat polyclonal antibody to PLK4.
Applications:
ELISA, WB
Reactivity:
Human
Immunogen:
Synthetic peptide corresponding to Human PLK4 (N terminal).
Sequence:
ATCIGEKIEDFKVGN
Host:
Goat
Clonality:
Polyclonal
Isotype:
IgG
Conjugate:
Unconjugated
Purification:
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Concentration:
100 µg at 0.5 mg/ml.
Product Form:
Liquid
Formulation:
Supplied in Tris Buffered Saline, pH 7.30, with 0.02% Sodium Azide and 0.5% BSA.
Storage:
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Target
Function:
Serine/threonine-protein kinase that plays a central role in centriole duplication. Able to trigger procentriole formation on the surface of the parental centriole cylinder, leading to the recruitment of centriole biogenesis proteins such as SASS6, CENPJ/CPAP, CCP110, CEP135 and gamma-tubulin. When overexpressed, it is able to induce centrosome amplification through the simultaneous generation of multiple procentrioles adjoining each parental centriole during S phase. Phosphorylates 'Ser-151' of FBXW5 during the G1/S transition, leading to inhibit FBXW5 ability to ubiquitinate SASS6. Its central role in centriole replication suggests a possible role in tumorigenesis, centrosome aberrations being frequently observed in tumors. Also involved in deuterosome-mediated centriole amplification in multiciliated that can generate more than 100 centrioles. Also involved in trophoblast differentiation by phosphorylating HAND1, leading to disrupt the interaction between HAND1 and MDFIC and activate HAND1. Phosphorylates CDC25C and CHEK2. Required for the recruitment of STIL to the centriole and for STIL-mediated centriole amplification (PubMed:22020124).
Involvement in Disease:
Microcephaly and chorioretinopathy, autosomal recessive, 2: A severe disorder characterized by microcephaly, delayed psychomotor development, growth retardation with dwarfism, and ocular abnormalities.
Sequence Similarities:
Belongs to the protein kinase superfamily. Ser/Thr protein kinase family. CDC5/Polo subfamily.
Post-Translational Modification:
Ubiquitinated; leading to its degradation by the proteasome.
Cellular Location:
Cytoplasm > Cytoskeleton > Microtubule organizing center > Centrosome > Centriole. Nucleus > Nucleolus. Cleavage furrow.
Component of the deuterosome, a structure that promotes de novo centriole amplification in multiciliated cells that can generate more than 100 centrioles. Associates with centrioles throughout the cell cycle. According to PubMed:16244668, it is not present at cleavage furrows.
Database Links:
Entrez Gene: 10733 Human
SwissProt: O00444 Human
Unigene: 172052 Human
Synonyms:
PLK 4 Antibody
PLK-4 Antibody
PLK4 Antibody
PLK4_HUMAN Antibody
Polo like Kinase 4 Antibody
Polo-like kinase 4 Antibody
Protein serine/threonine kinase Antibody
SAK Antibody
Serine/threonine kinase Antibody
Serine/Threonine Kinase 18 Antibody
Serine/threonine protein kinase 18 Antibody
Serine/threonine protein kinase PLK4 Antibody
Serine/threonine protein kinase Sak Antibody
Serine/threonine-protein kinase 18 Antibody
Serine/threonine-protein kinase PLK4 Antibody
Serine/threonine-protein kinase SAK Antibody
Snk Akin Kinase Antibody
STK 18 Antibody
STK18 Antibody
Information:
Target information shown above is from the UniProt Consortium.
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