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]

Overview

Recombinant protein of human hypothetical protein FLJ22167 (FLJ22167), transcript variant 3

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.