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FA2H antibody (AA 95-170)

FA2H Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6140410
  • Target See all FA2H Antibodies
    FA2H (Fatty Acid 2-Hydroxylase (FA2H))
    Binding Specificity
    • 7
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 95-170
    Reactivity
    • 29
    • 20
    • 13
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 23
    • 6
    Rabbit
    Clonality
    • 25
    • 4
    Polyclonal
    Conjugate
    • 17
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FA2H antibody is un-conjugated
    Application
    • 22
    • 10
    • 9
    • 2
    • 1
    Western Blotting (WB)
    Sequence
    NEPVALEETQ KTDPAMEPRF KVVDWDKDLV DWRKPLLWQV GHLGEKYDEW VHQPVTRPIR LFHSDLIEGL SKTVWY
    Cross-Reactivity
    Human, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 95-170 of human FA2H (NP_077282.3).
    Isotype
    IgG
    Top Product
    Discover our top product FA2H 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
    FA2H (Fatty Acid 2-Hydroxylase (FA2H))
    Alternative Name
    FA2H (FA2H Products)
    Background
    This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.,FA2H,FAAH,FAH1,FAXDC1,SCS7,SPG35,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Neuroscience,Cell Type Marker,Neuron marker,Axon marker,FA2H
    Molecular Weight
    18 kDa/42 kDa
    Gene ID
    79152
    UniProt
    Q7L5A8
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