QDPR antibody
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- Target See all QDPR Antibodies
- QDPR (Quinoid Dihydropteridine Reductase (QDPR))
- Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This QDPR antibody is un-conjugated
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogen
- Fusion protein of human QDPR
- Isotype
- IgG
- Top Product
- Discover our top product QDPR Primary Antibody
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- Application Notes
- WB 1:500-1:2000, IHC 1:50-1:200, ELISA 1:5000-1:10000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1.2 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- QDPR (Quinoid Dihydropteridine Reductase (QDPR))
- Alternative Name
- QDPR (QDPR Products)
- Synonyms
- DHPR antibody, PKU2 antibody, SDR33C1 antibody, 2610008L04Rik antibody, D5Ertd371e antibody, Dhpr antibody, QDPR antibody, qdpr antibody, MGC131372 antibody, DDBDRAFT_0168923 antibody, DDBDRAFT_0237752 antibody, DDB_0168923 antibody, DDB_0237752 antibody, CG4665 antibody, Dmel\\CG4665 antibody, si:ch211-89f22.2 antibody, quinoid dihydropteridine reductase antibody, quinoid dihydropteridine reductase S homeolog antibody, dihydropteridine reductase antibody, Dihydropteridine reductase antibody, bifunctional oxygen-insensitive NAD(P)H nitroreductase/dihydropteridine reductase NfnB antibody, quinoid dihydropteridine reductase a antibody, QDPR antibody, Qdpr antibody, qdpr antibody, qdpr.S antibody, Dhpr antibody, nfnB antibody, LOC5568428 antibody, dhpr antibody, qdpra antibody
- Background
- This gene encodes the enzyme dihydropteridine reductase, which catalyzes the NADH-mediated reduction of quinonoid dihydrobiopterin. This enzyme is an essential component of the pterin-dependent aromatic amino acid hydroxylating systems. Mutations in this gene resulting in QDPR deficiency include aberrant splicing, amino acid substitutions, insertions, or premature terminations. Dihydropteridine reductase deficiency presents as atypical phenylketonuria due to insufficient production of biopterin, a cofactor for phenylalanine hydroxylase.
- Molecular Weight
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Observed_MW: Refer to figures
Calculated_MW: 26 kDa
- UniProt
- P09417
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