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ALG12 Antibody

https://www.academycancerimmunology.org/web/image/product.template/3768/image_1920?unique=b611535
Size : 50 µL Clone Number: Aliases: 6-mannosyltransferase antibody; ALG12 antibody; ALG12_HUMAN antibody; Asparagine linked glycosylation 12 alpha 1 6 mannosyltransferase homolog antibody; Asparagine linked glycosylation protein 12 homolog antibody; Asparagine-linked glycosylation protein 12 homolog antibody; CDG1G antibody; Dol P Man: Man(7)GlcNAc(2) PP Dol alpha 1 6 mannosyltransferase antibody; Dol-P-Man: Man(7)GlcNAc(2)-PP-Dol alpha-1 antibody; Dolichyl P Man: Man(7)GlcNAc(2) PP dolichyl alpha 1 6 mannosyltransferase antibody; Dolichyl P mannose: Man 7 GlcNAc 2 PP dolichyl alpha 6 mannosyltransferase antibody; Dolichyl-P-Man: Man(7)GlcNAc(2)-PP-dolichyl-alpha-1 antibody; ECM39 antibody; hALG12 antibody; Mannosyltransferase ALG12 homolog antibody; Membrane protein SB87 antibody; MGC111358 antibody; MGC3136 antibody; PP14673 antibody Product Type: Polyclonal Antibody Immunogen Species: Homo sapiens (Human) UniProt ID: Q9BV10 Immunogen: Fusion protein of Human ALG12 Host: Rabbit Reactivity: Human, Mouse, Rat Tested Applications: ELISA, WB, IHC; ELISA: 1: 2000-1: 5000, WB: 1: 200-1: 1000, IHC: 1: 25-1: 100 Background: This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. Clonality: Polyclonal Isotype: IgG Purification Method: Antigen affinity purification Conjugate: Non-conjugated Buffer: -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol Form: Liquid Stroage: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. Target Names: ALG12 Research Areas: Metabolism;Signal transduction

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