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FH antibody (AA 411-510) (Biotin)

This anti-FH antibody is a Rabbit Polyclonal antibody detecting FH in ELISA, IHC (p) and IHC (fro). Suitable for Human.
Catalog No. ABIN751425

Quick Overview for FH antibody (AA 411-510) (Biotin) (ABIN751425)

Target

See all FH Antibodies
FH (Fumarate Hydratase (FH))

Reactivity

  • 73
  • 19
  • 17
  • 6
  • 1
  • 1
Human

Host

  • 60
  • 18
  • 2
Rabbit

Clonality

  • 61
  • 19
Polyclonal

Conjugate

  • 44
  • 7
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FH antibody is conjugated to Biotin

Application

  • 50
  • 28
  • 22
  • 19
  • 13
  • 13
  • 9
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  • 1
  • 1
ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Binding Specificity

    • 14
    • 8
    • 6
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
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    AA 411-510

    Predicted Reactivity

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

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human Fumarate hydratase (447-496aa)

    Isotype

    IgG
  • Application Notes

    IHC-P 1:200-400
    IHC-F 1:100-500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    Storage Comment

    Store at -20°C for 12 months.

    Expiry Date

    12 months
  • Target

    FH (Fumarate Hydratase (FH))

    Alternative Name

    Fumarate hydratase/FH

    Background

    Synonyms: mitochondrial, FH, Fumarase, Fumarate hydratase, Fumarate hydratase mitochondrial, FUMH_HUMAN, HLRCC, LRCC, MCL, MCUL 1, MCUL1, Multiple hereditary cutaneous leiomyomata.

    Background: Defects in FH are the cause of fumarase deficiency (FHD)also known as fumaricaciduria. FHD is characterized by progressive encephalopathy, developmental delay, hypotonia, cerebral atrophy and lactic and pyruvic acidemia.

    Gene ID

    2271
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