Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

ACSL4 antibody

ACSL4 Reactivity: Human WB, IP Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7265424
  • Target See all ACSL4 Antibodies
    ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))
    Reactivity
    • 61
    • 19
    • 19
    • 3
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 58
    • 2
    • 1
    Rabbit
    Clonality
    • 58
    • 3
    Monoclonal
    Conjugate
    • 27
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ACSL4 antibody is un-conjugated
    Application
    • 50
    • 24
    • 17
    • 15
    • 9
    • 9
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Purpose
    ACSL4 Rabbit mAb
    Sequence
    KLERFEIPIK VRLS
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human ACSL4.
    Isotype
    IgG
    Top Product
    Discover our top product ACSL4 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000,IP,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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
    ACSL4 (Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4))
    Alternative Name
    FACL4 (ACSL4 Products)
    Background
    The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants.,ACSL4,ACS4,FACL4,LACS4,MRX63,MRX68,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,FACL4
    Molecular Weight
    74kDa/79kDa
    Gene ID
    2182
    UniProt
    O60488
You are here:
Support