TMED5 anticorps (AA 33-164)

N° du produit ABIN7873987

Cet anticorps anti-TMED5 Polyclonal Lapin (ABIN7873987) détecte spécifiquement TMED5 dans WB, ELISA et IF. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour TMED5 anticorps (AA 33-164) (ABIN7873987)

Antigène: TMED5 (Transmembrane Emp24 Protein Transport Domain Containing 5 (TMED5))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMED5 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Détail du produit anti-TMED5 anticorps

Épitope: AA 33-164

Fonction: TMED5 Antibody / Transmembrane emp24 domain-containing protein 5

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids D33-K164) was used as the immunogen for the TMED5 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the TMED5 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the TMED5 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur TMED5

Antigène: TMED5 (Transmembrane Emp24 Protein Transport Domain Containing 5 (TMED5))

Autre désignation: TMED5

Sujet: Transmembrane emp24 domain-containing protein 5 is a protein that in humans is encoded by the TMED5 gene. TMED5 is a 229 amino acid single-pass type I membrane protein that belongs to the EMP24/GP25L family and contains one GOLD domain. The gene that encodes TMED5 contains nearly 31,000 bases and maps to human chromosome 1p22.1. As the largest human chromosome, chromosome 1 spans about 260 million base pairs and makes up approximately 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

UniProt: Q9Y3A6

Pathways: SARS-CoV-2 Protein Interactome