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Phenylalanine Hydroxylase antibody (AA 132-161)

This anti-Phenylalanine Hydroxylase antibody is a Rabbit Polyclonal antibody detecting Phenylalanine Hydroxylase in WB. Suitable for Human and Mouse.
Catalog No. ABIN651111

Quick Overview for Phenylalanine Hydroxylase antibody (AA 132-161) (ABIN651111)

Target

See all Phenylalanine Hydroxylase Antibodies
Phenylalanine Hydroxylase

Reactivity

  • 54
  • 25
  • 17
Human, Mouse

Host

  • 48
  • 7
  • 1
Rabbit

Clonality

  • 49
  • 7
Polyclonal

Conjugate

  • 33
  • 8
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Phenylalanine Hydroxylase antibody is un-conjugated

Application

  • 44
  • 23
  • 22
  • 9
  • 7
  • 6
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB)

Clone

RB24519
  • Binding Specificity

    • 6
    • 6
    • 5
    • 5
    • 4
    • 4
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 132-161

    Predicted Reactivity

    B, Rat

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This PAH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 132-161 amino acids from the Central region of human PAH.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    Phenylalanine Hydroxylase

    Alternative Name

    PAH

    Target Type

    Chemical

    Background

    PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.

    Molecular Weight

    51862

    Gene ID

    5053

    NCBI Accession

    NP_000268

    UniProt

    P00439
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