CEP152 Polyclonal Antibody

Uniprot : O94986
    • polyclonal antibody-Elabscience
    • polyclonal antibody-Elabscience
    • polyclonal antibody-Elabscience
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    • polyclonal antibody-Elabscience
    • polyclonal antibody-Elabscience
    • polyclonal antibody-Elabscience
    • polyclonal antibody-Elabscience
    • polyclonal antibody-Elabscience
    • polyclonal antibody-Elabscience

      Catalog number:E-AB-30880

      Synonyms:Asterless,CE152,Centrosomal protein 152kDa,Centrosomal protein of 152 kDa,Cep152,FLJ21594,KIAA0912,MCPH4,MCPH9,Microcephaly primary autosomal recessive 4,SCKL5

      Size:
      • 20μL
      • 60μL
      • 120μL
      • 200μL
      Qty:
      - +
      Price: $69

      Host: Rabbit

      Reactivity: H,M

      Applications: WB,IHC-p,ELISA

      Lead Time: 7~10 daysWelcome to order from local distributors.

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      Overview

      Synonyms Asterless,CE152,Centrosomal protein 152kDa,Centrosomal protein of 152 kDa,Cep152,FLJ21594,KIAA0912,MCPH4,MCPH9,Microcephaly primary autosomal recessive 4,SCKL5
      Swissprot O94986
      Source Rabbit
      Reactivity Human,Mouse
      Immunogen Synthesized peptide derived from the Internal region of human CEP152
      Application WB,IHC-p,ELISA
      Recommended dilution WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:40000
      Concentration 1mg/mL
      Clonality Polyclonal

      Properties

      Cellular localization Cytoplasm>cytoskeleton>centrosome.
      Isotype IgG
      Purification Affinity purification
      Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
      Storage buffer PBS with 0.02% sodium azide,0.5% BSA and 50% glycerol pH 7.4.
      Background This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants.CEP152 (Centrosomal Protein 152) is a Protein Coding gene. Diseases associated with CEP152 include Microcephaly 9, Primary, Autosomal Recessive and Seckel Syndrome 5. Among its related pathways are Regulation of PLK1 Activity at G2/M Transition and Organelle biogenesis and maintenance. GO annotations related to this gene include protein kinase binding.

      Images

      Western Blot analysis of HuvEc cells with CEP152 Polyclonal Antibody.

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