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TPI1 antibody (AA 1-286)

The Rabbit Polyclonal anti-TPI1 antibody is suitable to detect TPI1 in samples from Human, Mouse and Rat. It has been validated for WB, ELISA and FACS.
Catalog No. ABIN7869051
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for TPI1 antibody (AA 1-286) (ABIN7869051)

Target

See all TPI1 Antibodies
TPI1 (Triosephosphate Isomerase 1 (TPI1))

Reactivity

  • 70
  • 44
  • 32
  • 8
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 63
  • 10
  • 7
  • 3
Rabbit

Clonality

  • 62
  • 19
Polyclonal

Conjugate

  • 50
  • 9
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TPI1 antibody is un-conjugated

Application

  • 77
  • 29
  • 20
  • 19
  • 17
  • 14
  • 13
  • 13
  • 10
  • 7
  • 6
  • 6
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 9
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    AA 1-286

    Purpose

    TPI1 Antibody / Triosephosphate isomerase

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids M1-Q286) was used as the immunogen for the TPI1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the TPI1 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 TPI1 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

    TPI1 (Triosephosphate Isomerase 1 (TPI1))

    Alternative Name

    TPI1

    Background

    Triosephosphate isomerase is an enzyme that in humans is encoded by the TPI1 gene. This gene encodes an enzyme, consisting of two identical proteins, which catalyzes the isomerization of glyceraldehydes 3-phosphate (G3P) and dihydroxy-acetone phosphate (DHAP) in glycolysis and gluconeogenesis. Mutations in this gene are associated with triosephosphate isomerase deficiency. Pseudogenes have been identified on chromosomes 1, 4, 6 and 7. Alternative splicing results in multiple transcript variants.

    UniProt

    P60174

    Pathways

    Cell RedoxHomeostasis
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