TTC38 antibody (AA 267-469)

Catalog No. ABIN8045960

This Rabbit Polyclonal antibody specifically detects TTC38 in ELISA, WB, FACS, IF and ICC. It exhibits reactivity toward Human.

Quick Overview for TTC38 antibody (AA 267-469) (ABIN8045960)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TTC38 antibody is un-conjugated

Application: ELISA, Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF), Immunocytochemistry (ICC)

Grade: Carrier-free

Product Details anti-TTC38 Antibody

Binding Specificity: AA 267-469

Purpose: Anti-TTC38 Antibody

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

Characteristics: Anti-TTC38 Antibody. Tested in ELISA, IF, ICC, WB, Flow Cytometry applications. This antibody reacts with Human.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. 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

Molecular Weight: 53 kDa

Gene ID: 55020

UniProt: Q5R3I4