TMEM67 anticorps (Center)

N° du produit ABIN2856740

L’anticorps Lapin Polyclonal anti-TMEM67 a été validé pour WB. Il convient pour détecter TMEM67 dans des échantillons de Humain.

Aperçu rapide pour TMEM67 anticorps (Center) (ABIN2856740)

Antigène: TMEM67 (Transmembrane Protein 67 (TMEM67))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM67 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-TMEM67 anticorps

Épitope: Center

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

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