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ACSF3 antibody (AA 270-450)

ACSF3 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6136454
  • Target See all ACSF3 Antibodies
    ACSF3 (Acyl-CoA Synthetase Family Member 3 (ACSF3))
    Binding Specificity
    • 8
    • 6
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    AA 270-450
    Reactivity
    • 24
    • 11
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 22
    • 2
    Rabbit
    Clonality
    • 24
    Polyclonal
    Conjugate
    • 10
    • 4
    • 3
    • 3
    • 2
    • 2
    This ACSF3 antibody is un-conjugated
    Application
    • 19
    • 17
    • 14
    • 1
    Western Blotting (WB)
    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
    Top Product
    Discover our top product ACSF3 Primary Antibody
  • 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 (ACSF3 Products)
    Synonyms
    BB101783 antibody, acyl-CoA synthetase family member 3 antibody, ACSF3 antibody, Acsf3 antibody
    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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