TTC38 antibody (AA 267-469) (Biotin)

Catalog No. ABIN8045950

The Biotin-conjugated Rabbit Polyclonal anti-TTC38 antibody (ABIN8045950) specifically detects TTC38 in ELISA, WB and IHC. The antibody is reactive with Human samples.

Quick Overview for TTC38 antibody (AA 267-469) (Biotin) (ABIN8045950)

Target: TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TTC38 antibody is conjugated to Biotin

Application: ELISA, Western Blotting (WB), Immunohistochemistry (IHC)

Product Details anti-TTC38 Antibody (Biotin)

Binding Specificity: AA 267-469

Purpose: Anti-TTC38 Antibody Biotin Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human TTC38 recombinant protein (Position: E267-Q469).

Isotype: IgG

Application Details

Application Notes: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for TTC38

Target: TTC38 (Tetratricopeptide Repeat Domain 38 (TTC38))

Alternative Name: TTC38

Background:

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.

Gene Full Name: tetratricopeptide repeat domain 38

Gene ID: 55020

UniProt: Q5R3I4