PQBP1 (NM_001032381) Human Recombinant Protein
Product Specifications
Background
This gene encodes a nuclear polyglutamine-binding protein that is involved with transcription activation. The encoded protein contains a WW domain. Mutations in this gene have been found in patients with Renpenning syndrome 1 and other syndromes with X-linked cognitive disability. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.[provided by RefSeq, Nov 2009]
Synonyms
MRX2; MRX55; MRXS3; MRXS8; NPW38; RENS1; SHS
Gene ID
10084
UniProt
O60828, A0A0S2Z4V5
Accession Number mRNA
NM_001032381
Chromosomal Location
Xp11.23
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Spliceosome
Field of Research
Spliceosome
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
Transcription Factors
Molecular Weight
30.3 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
PQBP1
Species
Human
Protein ID
NP_001027553
Overview
Purified recombinant protein of Homo sapiens polyglutamine binding protein 1 (PQBP1), transcript variant 2
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/10084
Uniprot URL
https://www.uniprot.org/uniprot/O60828
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001032381
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001027553
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