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Anti-PEPD / PROLIDASE Antibody (aa1-494, PE) LS-C280747


Wt. Vol. Conc. Price
- 100 µl - $620
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)

Alternate Forms of this Antibody

LS-C328184 Unconjugated, Azide-free
LS-C280742 AP Conjugated
LS-C280743 APC Conjugated
LS-C280744 Biotin Conjugated
LS-C280745 FITC Conjugated
LS-C280746 HRP Conjugated, Azide-free

Most Popular PEPD / PROLIDASE Antibodies

Anti-PEPD / PROLIDASE Antibody (clone 1B7) IHC-plus™ LS-B11014
Mouse Monoclonal [clone 1B7] (IgG1) to Human PEPD / PROLIDASE
IHC - Paraffin, Immunofluorescence, Western blot, Flow Cytometry
Immunohistochemistry Image
Anti-PEPD / PROLIDASE Antibody (aa359-408) IHC-plus™ LS-B12732
Rabbit Polyclonal (IgG) to Human PEPD / PROLIDASE
Human, Mouse, Rat, Bat, Dog, Guinea pig, Horse, Pig
IHC - Paraffin, Western blot
Immunohistochemistry - Paraffin Image

100% Guaranteed 100% Guaranteed
Mouse Monoclonal (IgG1) to Human PEPD / PROLIDASE
ICC, Western blot, ELISA (applications tested for the base form of this product only)
PE Conjugated


Human (tested or 100% immunogen sequence identity)
IgG1 Monoclonal
Affinity purified


  • ICC
  • Western blot
  • (applications tested for the base form of this product only)

Specificity and Use

PEPD / PROLIDASE antibody was raised against recombinant human PEPD (aa1-494).
The applications listed have been tested for the base form of this product. Alternate forms, such as conjugated, azide-free, or ready-to-use, have not been tested.


PBS, pH 7.2, 0.09% sodium azide.
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for at least 6 months.
For research use only.


P12955 NM_000285 NP_000276.2

PEPD Antibody, Aminoacyl-L-proline hydrolase Antibody, Imidodipeptidase Antibody, PRD Antibody, PROLIDASE Antibody, X-Pro dipeptidase Antibody, Xaa-Pro dipeptidase Antibody, Peptidase D Antibody, Proline dipeptidase Antibody

PEPD / PROLIDASE is 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.

Requested From: United States
Date Requested: 10/28/2016

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