ALG3 Antikörper (AA 61-438)

Produktnummer ABIN7967716

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch ALG3 in FACS, ELISA und WB. Es zeigt Reaktivität gegenüber Proben von Human und Maus.

Kurzübersicht für ALG3 Antikörper (AA 61-438) (ABIN7967716)

Target: ALG3 (ALG3, alpha-1,3- mannosyltransferase (ALG3))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ALG3 Antikörper ist unkonjugiert

Applikation: Flow Cytometry (FACS), ELISA, Western Blotting (WB)

Güteklasse: Carrier-free

Produktdetails anti-ALG3 Antikörper

Bindungsspezifität: AA 61-438

Verwendungszweck: Anti-ALG3 Antibody

Kreuzreaktivität (Details): No cross-reactivity with other proteins.

Produktmerkmale: Anti-ALG3 Antibody. Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human ALG3 recombinant protein (Position: I61-H438).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Western blot, 0.25-0.5 μg/mL, Human, Mouse Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human ELISA, 0.1-0.5 μg/mL, -

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Konzentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Haltbarkeit: 12 months

Details zu ALG3

Target: ALG3 (ALG3, alpha-1,3- mannosyltransferase (ALG3))

Andere Bezeichnung: ALG3

Hintergrund:

Background: Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase is an enzyme that, in humans, is encoded by the ALG3 gene. This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene Full Name: ALG3 alpha-1,3- mannosyltransferase

Molekulargewicht: 50-55 kDa

Gen-ID: 10195

UniProt: Q92685