TTC38 anticorps (AA 267-469) (Biotin)

N° du produit ABIN8045950

Cet anticorps anti-TTC38 Polyclonal Lapin conjugué à Biotin (ABIN8045950) détecte spécifiquement TTC38 dans ELISA, WB et IHC. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour TTC38 anticorps (AA 267-469) (Biotin) (ABIN8045950)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TTC38 est conjugé à/à la Biotin

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

Détail du produit anti-TTC38 anticorps (Biotin)

Épitope: AA 267-469

Fonction: Anti-TTC38 Antibody Biotin Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Information d'application

Indications d'application: 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

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

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

Date de péremption: 12 months

Détails sur TTC38

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

Autre désignation: TTC38

Sujet:

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

ID gène: 55020

UniProt: Q5R3I4