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TTC38 antibody (AA 267-469)

This Rabbit Polyclonal antibody specifically detects TTC38 in ELISA, WB, FACS and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7873061
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for TTC38 antibody (AA 267-469) (ABIN7873061)

Target

See all TTC38 Antibodies
TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

Reactivity

  • 16
  • 9
Human

Host

  • 15
  • 1
Rabbit

Clonality

  • 16
Polyclonal

Conjugate

  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TTC38 antibody is un-conjugated

Application

  • 7
  • 5
  • 3
  • 1
  • 1
  • 1
ELISA, Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF)
  • Binding Specificity

    • 6
    • 1
    • 1
    AA 267-469

    Purpose

    TTC38 Antibody / Tetratricopeptide repeat protein 38

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids E267-Q469) was used as the immunogen for the TTC38 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the TTC38 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 TTC38 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

    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

    Alternative Name

    TTC38

    Background

    TTC38 (tetratricopeptide repeat domain 38) is a 469 amino acid protein that contains three TPR repeats and belongs to the TTC38 family. The gene that encodes TTC38 consists of over 26,000 bases and maps to 22q13. Housing over 500 genes, chromosome 22 is the second smallest chromosome in the human genome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. In addition, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

    UniProt

    Q5R3I4
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