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Kallikrein 4 peptide (Catalytic domain) (ab43086)

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Overview

  • Product nameKallikrein 4 peptide (Catalytic domain)See all Kallikrein 4 proteins and peptides ...
  • Protein descriptionThis peptide was used as an immunogen for ab40950 - Kallikrein 4 antibody - Catalytic domain.

    • Properties

  • Purity> 95 % by SDS-PAGE
  • FormLiquid
  • Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
  • Storage bufferPreservative: None
    Constituents: 0.001% Tween 20, 30mM HEPES, 2mM EDTA, 150mM Sodium chloride, pH 6.75
  • Concentration information loading...
  • Research Areas

    • Applications

    Our Abpromise guarantee covers the use of ab43086 in the following tested applications.

    The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

    Application Notes
    ELISA
    WB
  • Application notesELISA: Use at an assay dependent dilution. WB: Use at an assay dependent dilution. This peptide can be used with studies using ab40950. Dilution optimised using Chromogenic detection. Not yet tested in other applications. Optimal dilutions/concentrations should be determined by the end user.

    • Protein info

    • Alternative names
        7S nerve growth factor alpha chainAI2A1Alpha-NGF
        Androgen-regulated message 1ARM1EC 3.4.21.-EMSPEMSP 1EMSP1Enamel Matrix Serine Protease 1Enamel matrix serine proteinase 1HK4KallikreinKallikrein 1-related peptidase-like b4Kallikrein 4Kallikrein 4 (prostase, enamel matrix, prostate)Kallikrein L1Kallikrein like protein 1Kallikrein like protein 1Kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)Kallikrein-4Kallikrein-like protein 1Kallikrein-related peptidase 4KLK 4KLK L1KLK-L1KLK4KLK4_HUMANMGC116827MGC116828ProstaseProtease Serine 17PRSS 17PRSS17PSTSSerine protease 17
      see all
  • Tissue specificityExpressed in prostate.
  • Involvement in diseaseDefects in KLK4 are the cause of amelogenesis imperfecta hypomaturation type 2A1 (AI2A1) [MIM:204700]. AI2A1 is an autosomal recessive defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel.
  • Sequence similaritiesBelongs to the peptidase S1 family. Kallikrein subfamily.
    Contains 1 peptidase S1 domain.
  • Cellular localizationSecreted.

    • Target information above from: UniProt accession Q9Y5K2 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt

    References for Kallikrein 4 peptide (Catalytic domain) (ab43086)

    ab43086 has not yet been referenced specifically in any publications.

    Publishing research using ab43086 ? Please let us know so that we can cite the reference in this datasheet

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