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The antibody against GYG1 was raised in rabbit using the Human GYG1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
The antibody against GYG1 was raised in rabbit using the Human GYG1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
$600.00
| Cat.No | ADC-53166A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | GYG1 |
| Target Synonyms | Glycogenin antibody; Glycogenin-1 antibody; Glycogenin1 antibody; GLYG_HUMAN antibody; GN-1 antibody; GN1 antibody; GYG 1 antibody; GYG antibody; GYG1 antibody | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium Azide | Purification Method | Antigen affinity purified |
| Conjugate | Non-conjugated | Application | ELISA, WB |
| Storage | Upon receipt |
| Immunogen Description | Human GYG1 | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | P46976 |
Uniprot Id
P46976
Target Species
Human
Target Name
GYG1
Target Full Name
Glycogenin-1
Target Function
Self-glucosylates, via an inter-subunit mechanism, to form an oligosaccharide primer that serves as substrate for glycogen synthase.
Target Involvement
Glycogen storage disease 15 (GSD15); Polyglucosan body myopathy 2 (PGBM2)
Target Protein Families
Glycosyltransferase 8 family, Glycogenin subfamily
Target Tissue Specificity
Highly expressed in skeletal muscle and heart, with lower levels in brain, lung, kidney and pancreas.
Target Synonyms
Glycogenin; Glycogenin-1; Glycogenin1; GLYG_HUMAN; GN-1; GN1; GYG 1; GYG; GYG1
Target Background
This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.
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