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| Cat.No | ACP05773 | Target Name | ALG9 |
|---|---|---|---|
| Target Synonyms | 2-mannosyltransferase ALG9; Asparagine-linked glycosylation protein 9 homolog; Disrupted in bipolar disorder protein 1, ALG9; ALG9_HUMAN; Alpha-1 | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Protein Length | Partial |
| Purity | >85% (SDS-PAGE) | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q9H6U8 |
|---|
Uniprot Id
Q9H6U8
Target Species
Human
Target Name
ALG9
Target Full Name
Alpha-1,2-mannosyltransferase ALG9
Target Function
Catalyzes the transfer of mannose from Dol-P-Man to lipid-linked oligosaccharides.
Target Involvement
Congenital disorder of glycosylation 1L (CDG1L); Gillessen-Kaesbach-Nishimura syndrome (GIKANIS)
Target Subcellular Location
Endoplasmic reticulum membrane; Multi-pass membrane protein.
Target Protein Families
Glycosyltransferase 22 family
Target Tissue Specificity
Ubiquitously expressed; with highest levels in heart, liver and pancreas.
Target Synonyms
ALG9; ALG9_HUMAN; Alpha-1,2-mannosyltransferase ALG9; Asparagine-linked glycosylation protein 9 homolog; Disrupted in bipolar disorder protein 1
Target Background
This gene encodes an alpha-1, 2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene.
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