TMEM67 Antikörper (Center)

Produktnummer ABIN2856740

Der Kaninchen Polyklonal Anti-TMEM67-Antikörper wurde für WB validiert. Er ist geeignet, TMEM67 in Proben von Human zu detektieren.

Kurzübersicht für TMEM67 Antikörper (Center) (ABIN2856740)

Target: TMEM67 (Transmembrane Protein 67 (TMEM67))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TMEM67 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-TMEM67 Antikörper

Bindungsspezifität: Center

Kreuzreaktivität: Human

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

Aufreinigung: Purified by antigen-affinity chromatography.

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

Isotyp: IgG

Anwendungsinformationen

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

Kommentare:

Positive Control: H1299

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Thimerosal (Merthiolate)

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu TMEM67

Target: TMEM67 (Transmembrane Protein 67 (TMEM67))

Andere Bezeichnung: transmembrane protein 67

Hintergrund: 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

Molekulargewicht: 112 kDa

Gen-ID: 91147

UniProt: Q5HYA8