DATASHEET
Host:
Rabbit
Target Protein:
PRODH
Immunogen Range:
141-240/600
Clonality:
Polyclonal
Isotype:
IgG
Entrez Gene:
5625
Swiss Prot:
O43272
Source:
KLH conjugated synthetic peptide derived from human PRODH
Purification:
Purified by Protein A.
Storage Buffer:
0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage:
Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
Background:
Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
VALIDATION IMAGES
Formalin-fixed and paraffin embedded rat brain tissue labeled with Anti PRODH Polyclonal Antibody,Unconjugated (bs-5813R) at 1:200 followed by conjugation to the secondary antibody and DAB staining.
Formalin-fixed and paraffin embedded mouse kidney tissue labeled with Anti PRODH Polyclonal Antibody,Unconjugated (bs-5813R) at 1:200 followed by conjugation to the secondary antibody and DAB staining.
Paraformaldehyde-fixed, paraffin embedded Mouse brain; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with PRODH Polyclonal Antibody, Unconjugated (bs-5813R) at 1:400 overnight at 4°C, DAB staining.