TMEM67 Antikörper (Center)

Produktnummer ABIN2856740

Produktdetails anti-TMEM67 Antikörper

Target: TMEM67 (Transmembrane Protein 67 (TMEM67))

Bindungsspezifität: Center

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TMEM67 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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 (TMEM67 Produkte)

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

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