HPDL (NM_032756) Human Recombinant Protein
Product Specifications
Background
The protein encoded by this intronless gene localizes to mitochondria, where it may function as 4-hydroxyphenylpyruvate dioxygenase. Clinical studies have identified several bi-allelic variants in this gene that lower the level of the encoded protein and lead to a clinically variable form of pediatric-onset spastic movement disorder. [provided by RefSeq, Aug 2020]
Synonyms
4-HPPD-L; GLOXD1
Gene ID
84842
UniProt
Q96IR7
Accession Number mRNA
NM_032756
Chromosomal Location
1p34.1
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
39.2 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
HPDL
Species
Human
Protein ID
NP_116145
Overview
Recombinant protein of human 4-hydroxyphenylpyruvate dioxygenase-like (HPDL)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/84842
Uniprot URL
https://www.uniprot.org/uniprot/Q96IR7
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_032756
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_116145
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