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BSCL2 (NM_032667) Human Recombinant Protein

Product Specifications

Background

This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2) .[provided by RefSeq, Mar 2011]

Synonyms

GNG3LG; HMN5; HMN5C; PELD; SPG17

Gene ID

26580

UniProt

Q96G97, A0A024R549

Accession Number mRNA

NM_032667

Chromosomal Location

11q12.3

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

Function

Druggable Genome, Transmembrane

Molecular Weight

44.2 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

BSCL2

Species

Human

Protein ID

NP_116056

Overview

Recombinant protein of human Bernardinelli-Seip congenital lipodystrophy 2 (seipin) (BSCL2), transcript variant 2

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/26580

Uniprot URL

https://www.uniprot.org/uniprot/Q96G97

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_032667

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_116056

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