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TYR antibody (AA 130-529)

This Rabbit Polyclonal antibody specifically detects TYR in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN7870496
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for TYR antibody (AA 130-529) (ABIN7870496)

Target

See all TYR Antibodies
TYR (Tyrosinase (TYR))

Reactivity

  • 139
  • 25
  • 23
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 87
  • 57
Rabbit

Clonality

  • 86
  • 59
Polyclonal

Conjugate

  • 73
  • 8
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TYR antibody is un-conjugated

Application

  • 68
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  • 23
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  • 20
  • 14
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Western Blotting (WB), ELISA
  • Binding Specificity

    • 15
    • 7
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
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    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 130-529

    Purpose

    TYR Antibody / Tyrosinase

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids E130-K529) was used as the immunogen for the TYR antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the TYR 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 TYR 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

    TYR (Tyrosinase (TYR))

    Alternative Name

    TYR

    Background

    The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.

    UniProt

    P14679
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