TCTN3 anticorps (PE)

N° du produit ABIN1712707

Cet anticorps Lapin Polyclonal détecte spécifiquement TCTN3 dans WB. Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour TCTN3 anticorps (PE) (ABIN1712707)

Antigène: TCTN3 (Tectonic Family Member 3 (TCTN3))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TCTN3 est conjugé à/à la PE

Application: Western Blotting (WB)

Détail du produit anti-TCTN3 anticorps (PE)

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human TCTN3/TECT3

Isotype: IgG

Information d'application

Indications d'application: FCM(1:20-100)

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur TCTN3

Antigène: TCTN3 (Tectonic Family Member 3 (TCTN3))

Autre désignation: Tctn3/Tect3

Sujet:

Synonyms: C10orf61, Chromosome 10 open reading frame 61, DKFZP564D116, TCTN3, TECT3_HUMAN, Tectonic 3, Tectonic 3 precursor, Tectonic family member 3, Tectonic-3.

Background: Tect3 is a 607 amino acid single-pass type I membrane protein that belongs to the tectonic family and exists as four alternatively spliced isoforms. Tect3 interacts with MKS1 and may be involved in apoptosis regulation. The gene that encodes Tect3 contains approximately 31,560 bases and maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs and encoding nearly 1,200 genes, chromosome 10 makes up approximately 4.5 % of the human genome. Several protein-coding genes, including those that encode chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, Cockayne syndrome, multiple endocrine neoplasia type 2 and porphyria. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10.

ID gène: 26123