TMED5 Antikörper (AA 33-164)

Produktnummer ABIN7873987

Der Kaninchen Polyklonal anti-TMED5 Antikörper (ABIN7873987) detektiert spezifisch TMED5 in WB, ELISA und IF. Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus und Ratte.

Kurzübersicht für TMED5 Antikörper (AA 33-164) (ABIN7873987)

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TMED5 Antikörper ist unkonjugiert

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

Produktdetails anti-TMED5 Antikörper

Bindungsspezifität: AA 33-164

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

Aufreinigung: Antigen affinity purified

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the TMED5 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu TMED5

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

Andere Bezeichnung: TMED5

Hintergrund: 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 Interaktom