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PEPD antibody (AA 288-424)

The Rabbit Polyclonal anti-PEPD antibody has been validated for WB. It is suitable to detect PEPD in samples from Human.
Catalog No. ABIN6145446

Quick Overview for PEPD antibody (AA 288-424) (ABIN6145446)

Target

See all PEPD Antibodies
PEPD (Peptidase D (PEPD))

Reactivity

  • 40
  • 13
  • 13
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 33
  • 7
Rabbit

Clonality

  • 33
  • 7
Polyclonal

Conjugate

  • 23
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This PEPD antibody is un-conjugated

Application

  • 22
  • 12
  • 9
  • 6
  • 4
  • 4
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 288-424

    Sequence

    ITCSFPANGK FTADQKAVYE AVLRSSRAVM GAMKPGVWWP DMHRLADRIH LEELAHMGIL SGSVDAMVQA HLGAVFMPHG LGHFLGIDVH DVGGYPEGVE RIDEPGLRSL RTARHLQPGM VLTVEPGIYF IDHLLDE

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 288-424 of human PEPD (NP_000276.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    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.,PEPD,PROLIDASE,Signal Transduction,Cell Biology & Developmental Biology,Ubiquitin,Endocrine & Metabolism,Amino acid metabolism,PEPD

    Molecular Weight

    47 kDa/49 kDa/54 kDa

    Gene ID

    5184

    UniProt

    P12955
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