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PHF8 antibody (AA 501-600)

The Rabbit Polyclonal anti-PHF8 antibody has been validated for FACS and ELISA. It is suitable to detect PHF8 in samples from Human.
Catalog No. ABIN873332

Quick Overview for PHF8 antibody (AA 501-600) (ABIN873332)

Target

See all PHF8 Antibodies
PHF8 (PHD Finger Protein 8 (PHF8))

Reactivity

  • 32
  • 15
  • 8
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 35
  • 1
Rabbit

Clonality

  • 32
  • 4
Polyclonal

Conjugate

  • 14
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PHF8 antibody is un-conjugated

Application

  • 13
  • 13
  • 7
  • 6
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS), ELISA
  • Binding Specificity

    • 15
    • 3
    • 2
    • 2
    AA 501-600

    Cross-Reactivity

    Human

    Predicted Reactivity

    Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human PHF8

    Isotype

    IgG
  • Application Notes

    ELISA 1:500-1000
    FCM 1:20-100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    Expiry Date

    12 months
  • Target

    PHF8 (PHD Finger Protein 8 (PHF8))

    Alternative Name

    Phf8

    Background

    Synonyms: PHD finger protein 8, PHD finger protein 8, Histone lysine demethylase PHF8, PHD finger protein 8, PHF8, PHF8_HUMAN, ZNF422.

    Background: The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. Defects in this gene are a cause of mental retardation syndromic X-linked Siderius type (MRXSSD). Four transcript variants encoding different isoforms have been found for this gene.

    Gene ID

    23133
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