TMED5 antibody (AA 33-164)

Catalog No. ABIN7873987

The Rabbit Polyclonal anti-TMED5 antibody (ABIN7873987) specifically detects TMED5 in WB, ELISA and IF. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for TMED5 antibody (AA 33-164) (ABIN7873987)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TMED5 antibody is un-conjugated

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

Product Details anti-TMED5 Antibody

Binding Specificity: AA 33-164

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

Purification: Antigen affinity purified

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

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Lyophilized

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

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for TMED5

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

Alternative Name: TMED5

Background: 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