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PEPD antibody

PEPD Reactivity: Human, Mouse, Rat WB, IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7247249
  • Target See all PEPD Antibodies
    PEPD (Peptidase D (PEPD))
    Reactivity
    • 35
    • 11
    • 11
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 29
    • 6
    Rabbit
    Clonality
    • 31
    • 4
    Polyclonal
    Conjugate
    • 18
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    This PEPD antibody is un-conjugated
    Application
    • 17
    • 10
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human PEPD
    Isotype
    IgG
    Top Product
    Discover our top product PEPD Primary Antibody
  • Application Notes
    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.2 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    PEPD (Peptidase D (PEPD))
    Alternative Name
    PEPD (PEPD Products)
    Synonyms
    MGC89151 antibody, DDBDRAFT_0190220 antibody, DDBDRAFT_0266378 antibody, DDB_0190220 antibody, DDB_0266378 antibody, PROLIDASE antibody, cb1000 antibody, fj78g11 antibody, wu:fj78g11 antibody, prolidase antibody, Pep-4 antibody, Pep4 antibody, peptidase D antibody, peptidase D L homeolog antibody, pepd antibody, pepD antibody, PEPD antibody, pepd.L antibody, Pepd antibody
    Background
    This gene encodes a member of the peptidase family. The protein forms a homodimer that hydrolyzes dipeptides or tripeptides with C-terminal proline or hydroxyproline residues. The enzyme serves an important role in the recycling of proline, and may be rate limiting for the production of collagen. Mutations in this gene result in prolidase deficiency, which is characterized by the excretion of large amount of di- and tri-peptides containing proline. Multiple transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 55 kDa

    UniProt
    P12955
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