RD3 (NM_183059) Human Recombinant Protein
Product Specifications
Background
This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Overview
Recombinant protein of human retinal degeneration 3 (RD3)
Synonyms
C1orf36; LCA12
Gene ID
343035
UniProt
Q7Z3Z2
Accession Number mRNA
NM_183059
Chromosomal Location
1q32.3
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
22.5 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
RD3
Species
Human
Protein ID
NP_898882
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/343035
Uniprot URL
https://www.uniprot.org/uniprot/Q7Z3Z2
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_183059
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_898882
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