ARG40851

anti-PEPD antibody

anti-PEPD antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes PEPD
Tested Reactivity Hu
Predict Reactivity Hu, Ms, Rat, Cow, Dog, Goat, Gpig, Hrs, Rb, Zfsh
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name PEPD
Antigen Species Human
Immunogen Synthetic peptide around the middle region of Human PEPD (within the following region: LGAVFMPHGLGHFLGIDVHDVGGYPEGVERIDEPGLRSLRTARHLQPGMV).
Conjugation Un-conjugated
Alternate Names Peptidase D; X-Pro dipeptidase; Imidodipeptidase; EC 3.4.13.9; Prolidase; Xaa-Pro dipeptidase; Proline dipeptidase; PROLIDASE

Application Instructions

Predict Reactivity Note Predicted Homology Based On Immunogen Sequence: Cow: 92%; Dog: 100%; Goat: 79%; Guinea pig: 100%; Horse: 100%; Mouse: 100%; Rabbit: 93%; Rat: 100%; Zebrafish: 86%
Application Suggestion
Tested Application Dilution
IHC-P1:100
WB0.2 - 1 µg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity purified.
Buffer PBS, 0.09% (w/v) Sodium azide and 2% Sucrose.
Preservative 0.09% (w/v) Sodium azide
Stabilizer 2% Sucrose
Concentration Batch dependent: 0.5 - 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 5184 Human PEPD

Swiss-port # P12955 Human Xaa-Pro dipeptidase

Gene Symbol PEPD
Gene Full Name peptidase D
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.[provided by RefSeq, Oct 2009]
Function Splits dipeptides with a prolyl or hydroxyprolyl residue in the C-terminal position. Plays an important role in collagen metabolism because the high level of iminoacids in collagen. [UniProt]
Calculated MW 55 kDa