CCDC115 anticorps (AA 1-180) (HRP)

N° du produit ABIN7980902

Cet anticorps anti-CCDC115 Polyclonal Lapin conjugué à HRP (ABIN7980902) détecte spécifiquement CCDC115 dans WB, ELISA et IHC. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour CCDC115 anticorps (AA 1-180) (HRP) (ABIN7980902)

Antigène: CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC115 est conjugé à/à la HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Détail du produit anti-CCDC115 anticorps (HRP)

Épitope: AA 1-180

Fonction: Anti-CCDC115 Antibody HRP Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human CCDC115 recombinant protein (Position: M1-A180).

Isotype: IgG

Information d'application

Indications d'application: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur CCDC115

Antigène: CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

Autre désignation: CCDC115

Sujet:

Background: Coiled-coil domain containing 115 is a protein that in humans is encoded by the CCDC115 gene. 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) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans.

Gene Full Name: vacuolar ATPase assembly factor VMA22

ID gène: 84317

UniProt: Q96NT0