Comparison

Recombinant Human Dihydropteridine Reductase/QDPR Protein (His Tag)

Item no. ELS-PKSH032355-10ug
Manufacturer Elabscience
Amount 10ug
Category
Type Proteins
Specific against Human
Host Human Cells
ECLASS 10.1 32160409
ECLASS 11.0 32160409
UNSPSC 12352202
Alias Dihydropteridine Reductase, HDHPR, Quinoid Dihydropteridine Reductase, QDPR, DHPR
Similar products QDPR, DHPR, Quinoid Dihydropteridine Reductase, HDHPR, Dihydropteridine Reductase
Available
Synonym
Dihydropteridine Reductase, HDHPR, Quinoid Dihydropteridine Reductase, QDPR, DHPR
Storage
according to manual
Protein Construction
Recombinant Human Dihydropteridine Reductase is produced by our Mammalian expression system and the target gene encoding Ala2-Phe244 is expressed with a 6His tag at the C-terminus.
Sequence
Ala2-Phe244
Fusion tag
C-6His
Accession
P09417
Shipping
This product is provided as lyophilized powder which is shipped with ice packs.
Purity
> 95 % as determined by reducing SDS-PAGE.
Endotoxin
< 1.0 EU per ug as determined by the LAL method.
Stability and Storage
Lyophilized proteins are stable for up to 12 months when stored at -20 to -80CC. Reconstituted protein solution can be stored at 4-8C for 2-7 days. Aliquots of reconstituted samples are stable at < -20C for 3 months.
Mol Mass
26.8 kDa
AP Mol Mass
29 kDa
Formulation
Lyophilized from a 0.2 um filtered solution of 20mM TrisHCl, pH8.0.
Reconstitution
Please refer to the printed manual for detailed information.
Background
Dihydropteridine reductase, also known as HDHPR and Quinoid dihydropteridine reductase, QDPR and DHPR, belongs to the short-chain dehydrogenases/reductases (SDR) family. QDPR exists as a homodimer. QDPR is part of the pathway that recycles a substance called tetrahydrobiopterin, also known as BH4 and tryptophan hydroxylases. The regeneration of this substance is critical for the proper processing of several other amino acids in the body. Tetrahydrobiopterin also helps produce certain chemicals in the brain called neurotransmitters, which transmit signals between nerve cells. Defects in QDPR are the cause of BH4-deficient hyperphenylalaninemia type C (HPABH4C) which is a rare autosomal recessive disorder and is lethal.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 10ug
Available: In stock
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