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SLC27A3 antibody (AA 192-683)

The Rabbit Polyclonal anti-SLC27A3 antibody is suitable to detect SLC27A3 in samples from Human and Mouse. It has been validated for WB, ELISA and IHC (p).
Catalog No. ABIN7871676
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SLC27A3 antibody (AA 192-683) (ABIN7871676)

Target

See all SLC27A3 (FATP3) Antibodies
SLC27A3 (FATP3) (Fatty Acid Transport Protein 3 (FATP3))

Reactivity

  • 21
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 18
  • 3
Rabbit

Clonality

  • 19
  • 2
Polyclonal

Conjugate

  • 15
  • 2
  • 1
  • 1
  • 1
  • 1
This SLC27A3 antibody is un-conjugated

Application

  • 17
  • 15
  • 11
  • 2
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 8
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 192-683

    Purpose

    FATP-3 Antibody / ACSVL3 / SLC27A3

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids L192-I683) was used as the immunogen for the FATP-3 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the FATP-3 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the FATP-3 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    SLC27A3 (FATP3) (Fatty Acid Transport Protein 3 (FATP3))

    Alternative Name

    FATP-3

    Background

    Long-chain fatty acid transport protein 3 is a protein that in humans is encoded by the SLC27A3 gene. This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants.

    UniProt

    Q5K4L6
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