TMEM176A anticorps

N° du produit ABIN7075995

Détail du produit anti-TMEM176A anticorps

Antigène: TMEM176A (Transmembrane Protein 176A (TMEM176A))

Reactivité: Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM176A est non-conjugé

Application: Immunofluorescence (IF), Immunohistochemistry (IHC)

Réactivité croisée: Rat

Purification: Affinity purification

Immunogène: KLH conjugated Synthetic peptide corresponding to Mouse TMEM176A

Information d'application

Indications d'application: IHC/IF (R) 1:500-1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS, pH 7.4, 0.02 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Détails sur TMEM176A

Antigène: TMEM176A (Transmembrane Protein 176A (TMEM176A))

Autre désignation: TMEM176A (TMEM176A Produits)

Synonymes: anticorps GS188, anticorps HCA112, anticorps 0610011I04Rik, anticorps AU040201, anticorps AU041743, anticorps Keg2, anticorps 0610011i04rik, anticorps RGD1310725, anticorps CL1, anticorps transmembrane protein 176A, anticorps TMEM176A, anticorps Tmem176a

Sujet: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.

ID gène: 66058

UniProt: Q9DCS1