PTDSS1 (NM_014754) Human Recombinant Protein
Product Specifications
Background
The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
Overview
Recombinant protein of human phosphatidylserine synthase 1 (PTDSS1)
Synonyms
LMHD; PSS1; PSSA
Gene ID
9791
UniProt
P48651
Accession Number mRNA
NM_014754
Chromosomal Location
8q22.1
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Glycerophospholipid metabolism, Metabolic pathways
Field of Research
Glycerophospholipid metabolism, Metabolic pathways
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
55.3 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
PTDSS1
Species
Human
Protein ID
NP_055569
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/9791
Uniprot URL
https://www.uniprot.org/uniprot/P48651
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_014754
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_055569
Frequently Asked Questions
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