TMEM67 anticorps (Center)

N° du produit ABIN2856740

Détail du produit anti-TMEM67 anticorps

Antigène: TMEM67 (Transmembrane Protein 67 (TMEM67))

Épitope: Center

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM67 est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée: Humain

Attributs du produit: Rabbit polyclonal antibody to Meckelin (transmembrane protein 67)
meckelin isoform 1 antibody [N2C1], Internal

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human meckelin isoform 1. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: H1299

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur TMEM67

Antigène: TMEM67 (Transmembrane Protein 67 (TMEM67))

Autre désignation: transmembrane protein 67 (TMEM67 Produits)

Synonymes: anticorps JBTS6, anticorps MECKELIN, anticorps MKS3, anticorps NPHP11, anticorps TNEM67, anticorps 5330408M12Rik, anticorps B230117O07, anticorps b2b1163.1Clo, anticorps b2b1291.1Clo, anticorps Wpk, anticorps transmembrane protein 67, anticorps TMEM67, anticorps tmem67, anticorps Tmem67

Sujet: The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).

Cellular Localization: Cell membrane, Multi-pass membrane protein

Poids moléculaire: 112 kDa

ID gène: 91147

UniProt: Q5HYA8