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
Curated Selection
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