TMEM199 anticorps (AA 20-129)

N° du produit ABIN7871835

L’anticorps anti-TMEM199 Polyclonal Lapin est utilisé pour la détection de TMEM199 dans des échantillons de Humain. Il a été validé pour WB et ELISA.

Aperçu rapide pour TMEM199 anticorps (AA 20-129) (ABIN7871835)

Antigène: TMEM199 (Transmembrane Protein 199 (TMEM199))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM199 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-TMEM199 anticorps

Épitope: AA 20-129

Fonction: TMEM199 Antibody

Purification: Antigen affinity purified

Immunogène: Amino acids E20-H129 from the human protein were used as the immunogen for the TMEM199 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the TMEM199 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 TMEM199 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 TMEM199

Antigène: TMEM199 (Transmembrane Protein 199 (TMEM199))

Autre désignation: TMEM199

Sujet: TMEM199 encodes a protein homologous to the yeast V-ATPase assembly factor Vma12 and appears to be involved in Golgi homeostasis. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) in some human cells. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. By genomic sequence analysis, the TMEM199 gene is mapped to chromosome 17q11.1.

UniProt: Q8N511