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TTC38 antibody

TTC38 Reactivity: Human, Mouse ELISA, IHC, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7253539
  • Target See all TTC38 Antibodies
    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))
    Reactivity
    Human, Mouse
    Host
    • 13
    • 1
    Rabbit
    Clonality
    • 14
    Polyclonal
    Conjugate
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TTC38 antibody is un-conjugated
    Application
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human TTC38
    Isotype
    IgG
    Top Product
    Discover our top product TTC38 Primary Antibody
  • Application Notes
    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))
    Alternative Name
    TTC38 (TTC38 Products)
    Synonyms
    9030019H09 antibody, fb96d09 antibody, si:ch211-249g22.2 antibody, wu:fb96d09 antibody, zgc:112407 antibody, tetratricopeptide repeat domain 38 antibody, tetratricopeptide repeat domain 38 S homeolog antibody, TTC38 antibody, Ttc38 antibody, ttc38.S antibody, ttc38 antibody
    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.
    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 53 kDa

    UniProt
    Q5R3I4
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