TSPYL1 (NM_003309) Human Recombinant Protein
Product Specifications
Background
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT) . [provided by RefSeq, Dec 2009]
Overview
Recombinant protein of human TSPY-like 1 (TSPYL1)
Synonyms
TSPYL
Gene ID
7259
UniProt
Q9H0U9
Accession Number mRNA
NM_003309
Chromosomal Location
6q22.1
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
Molecular Weight
49 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
TSPYL1
Species
Human
Protein ID
NP_003300
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/7259
Uniprot URL
https://www.uniprot.org/uniprot/Q9H0U9
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_003309
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_003300
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