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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]

Overview

Recombinant protein of human 4-hydroxyphenylpyruvate dioxygenase-like (HPDL)

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

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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