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HSD17B4 antibody (AA 18-231)

This Rabbit Polyclonal antibody specifically detects HSD17B4 in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN1886119

Quick Overview for HSD17B4 antibody (AA 18-231) (ABIN1886119)

Target

See all HSD17B4 Antibodies
HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))

Reactivity

  • 38
  • 24
  • 15
  • 15
  • 8
  • 2
Human

Host

  • 49
  • 4
Rabbit

Clonality

  • 49
  • 4
Polyclonal

Conjugate

  • 27
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HSD17B4 antibody is un-conjugated

Application

  • 45
  • 17
  • 17
  • 13
  • 13
  • 12
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 18-231

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 18 and 231 of MFE-2
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))

    Alternative Name

    MFE-2

    Background

    The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids.It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids.Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD).An apparent pseudogene of this gene is present on chromosome 8.[provided by RefSeq]

    Molecular Weight

    80 kDa

    Gene ID

    3295

    Pathways

    Monocarboxylic Acid Catabolic Process
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