PRCD (NM_001077620) Human Recombinant Protein
Product Specifications
Background
This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]
Overview
Recombinant protein of human progressive rod-cone degeneration (PRCD)
Synonyms
RP36
Gene ID
768206
UniProt
Q00LT1
Accession Number mRNA
NM_001077620
Chromosomal Location
17q25.1
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Molecular Weight
5.8 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
PRCD
Species
Human
Protein ID
NP_001071088
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/768206
Uniprot URL
https://www.uniprot.org/uniprot/Q00LT1
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001077620
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001071088
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