TMEM231 (NM_001077419) Human Recombinant Protein
Product Specifications
Background
This gene encodes a transmembrane protein, which is a component of the B9 complex involved in the formation of the diffusion barrier between the cilia and plasma membrane. Mutations in this gene cause Joubert syndrome (JBTS) . Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]
Synonyms
ALYE870; JBTS20; PRO1886
Gene ID
79583
UniProt
Q9H6L2
Accession Number mRNA
NM_001077419
Chromosomal Location
16q23.1
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
Function
Transmembrane
Molecular Weight
22.7 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
TMEM231
Species
Human
Protein ID
NP_001070887
Overview
Recombinant protein of human hypothetical protein FLJ22167 (FLJ22167), transcript variant 3
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/79583
Uniprot URL
https://www.uniprot.org/uniprot/Q9H6L2
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001077419
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001070887
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