FAM161A (NM_032180) Human Recombinant Protein
Selected Variant
PH35974M5
Size: 20 µg
Product Specifications
Background
This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011]
Overview
Recombinant protein of human family with sequence similarity 161, member A (FAM161A)
Synonyms
RP28
Gene ID
84140
UniProt
Q3B820
Accession Number mRNA
NM_032180
Chromosomal Location
2p15
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
64.7 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
FAM161A
Species
Human
Protein ID
NP_115556
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/84140
Uniprot URL
https://www.uniprot.org/uniprot/Q3B820
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_032180
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_115556
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