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TSHZ1 antibody (AA 97-800)

The Rabbit Polyclonal anti-TSHZ1 antibody is suitable to detect TSHZ1 in samples from Human. It has been validated for WB, ELISA and IF.
Catalog No. ABIN7877274
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for TSHZ1 antibody (AA 97-800) (ABIN7877274)

Target

See all TSHZ1 Antibodies
TSHZ1 (Teashirt Zinc Finger Homeobox 1 (TSHZ1))

Reactivity

  • 23
  • 16
  • 4
Human

Host

  • 21
  • 2
Rabbit

Clonality

  • 22
  • 1
Polyclonal

Conjugate

  • 18
  • 1
  • 1
  • 1
  • 1
  • 1
This TSHZ1 antibody is un-conjugated

Application

  • 19
  • 15
  • 7
  • 5
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF)
  • Binding Specificity

    • 7
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 97-800

    Purpose

    TSHZ1 Antibody / Teashirt homolog 1

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids K97-R800) was used as the immunogen for the TSHZ1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the TSHZ1 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 TSHZ1 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

    TSHZ1 (Teashirt Zinc Finger Homeobox 1 (TSHZ1))

    Alternative Name

    TSHZ1

    Background

    Teashirt zinc finger homeobox 1 is a protein that in humans is encoded by the TSHZ1 gene. This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome.

    UniProt

    Q6ZSZ6
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