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QDPR antibody (AA 1-244)

This anti-QDPR antibody is a Rabbit Polyclonal antibody detecting QDPR in WB. Suitable for Human.
Catalog No. ABIN6146531

Quick Overview for QDPR antibody (AA 1-244) (ABIN6146531)

Target

See all QDPR Antibodies
QDPR (Quinoid Dihydropteridine Reductase (QDPR))

Reactivity

  • 39
  • 18
  • 8
Human

Host

  • 33
  • 5
  • 2
Rabbit

Clonality

  • 36
  • 4
Polyclonal

Conjugate

  • 18
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This QDPR antibody is un-conjugated

Application

  • 23
  • 16
  • 10
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 9
    • 7
    • 5
    • 2
    • 1
    AA 1-244

    Sequence

    MAAAAAAGEA RRVLVYGGRG ALGSRCVQAF RARNWWVASV DVVENEEASA SIIVKMTDSF TEQADQVTAE VGKLLGEEKV DAILCVAGGW AGGNAKSKSL FKNCDLMWKQ SIWTSTISSH LATKHLKEGG LLTLAGAKAA LDGTPGMIGY GMAKGAVHQL CQSLAGKNSG MPPGAAAIAV LPVTLDTPMN RKSMPEADFS SWTPLEFLVE TFHDWITGKN RPSSGSLIQV VTTEGRTELT PAYF

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-244 of human QDPR (NP_000311.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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.
  • Target

    QDPR (Quinoid Dihydropteridine Reductase (QDPR))

    Alternative Name

    QDPR

    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.,QDPR,DHPR,PKU2,SDR33C1,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,QDPR

    Molecular Weight

    22 kDa/25 kDa

    Gene ID

    5860

    UniProt

    P09417
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