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ACSF3 antibody (AA 270-450)

This anti-ACSF3 antibody is a Rabbit Polyclonal antibody detecting ACSF3 in WB. Suitable for Human.
Catalog No. ABIN6136454

Quick Overview for ACSF3 antibody (AA 270-450) (ABIN6136454)

Target

See all ACSF3 Antibodies
ACSF3 (Acyl-CoA Synthetase Family Member 3 (ACSF3))

Reactivity

  • 18
  • 10
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 16
  • 2
Rabbit

Clonality

  • 18
Polyclonal

Conjugate

  • 9
  • 3
  • 2
  • 2
  • 1
  • 1
This ACSF3 antibody is un-conjugated

Application

  • 13
  • 12
  • 9
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 270-450

    Sequence

    FSPQQVWEKF LSSETPRINV FMAVPTIYTK LMEYYDRHFT QPHAQDFLRA VCEEKIRLMV SGSAALPLPV LEKWKNITGH TLLERYGMTE IGMALSGPLT TAVRLPGSVG TPLPGVQVRI VSENPQREAC SYTIHAEGDE RGTKVTPGFE EKEGELLVRG PSVFREYWNK PEETKSAFTL D

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 270-450 of human ACSF3 (NP_001230208.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    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

    ACSF3 (Acyl-CoA Synthetase Family Member 3 (ACSF3))

    Alternative Name

    ACSF3

    Background

    This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene.,ACSF3,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Hydrolysis,Lipases,Cardiovascular,Lipids,ACSF3

    Molecular Weight

    64 kDa

    Gene ID

    197322

    UniProt

    Q4G176
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