ALG2 Rabbit Polyclonal Antibody
Other products for "ALG2"
Specifications
Product Data | |
Applications | WB |
Recommended Dilution | Western blotting (0.2 - 1.0 µg/ml) |
Reactivities | Bovine, Canine, Human, Mouse, Porcine, Rat, African clawed frog |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | Synthetic peptide directed towards the C terminal of human ALG2 |
Formulation | State: Aff - Purified State: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose. Note that this product is shipped as lyophilized powder to China customers. |
Purification | Purified using peptide immunoaffinity column |
Conjugation | Unconjugated |
Storage | Store undiluted at 2-8°C for one month or (in aliquots) at -20°C to -80°C for longer. Avoid repeated freezing and thawing. |
Stability | Shelf life: one year from despatch. |
Gene Name | ALG2, alpha-1,3/1,6-mannosyltransferase |
Database Link | |
Background | ALG2 is a member of the glycosyltransferase 1 family. It acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii).This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). |
Synonyms | CDGIi; FLJ14511; hALPG2; NET38 |
Reference Data | |
Protein Pathways | Metabolic pathways, N-Glycan biosynthesis |
Documents
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complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.