Asparagine-Linked Glycosylation 12, alpha-1,6-Mannosyltransferase Homolog (S. Cerevisiae) (ALG12) antibody
| Antigen | Asparagine-Linked Glycosylation 12, alpha-1,6-Mannosyltransferase Homolog (S. Cerevisiae) (ALG12) |
| Synonyms | ECM39, hALG12, MGC3136, PP14673, MGC111358, MGC29374, ALG12, si:dkey-164m14.3 |
| Clonality | Monoclonal (5E3) |
| Host |
Mouse |
| Reactivity |
Human |
| Application |
ELISA, Western Blotting (WB)
|
![]() |
5 references available |
| Certificates | ISO 9001:2008 |
| Catalog no. | ABIN393387 |
| Quantity | 0.1mg (1 mg/ml) |
| Price | 450.00 $ Plus shipping costs $45.00 |
| Shipping to |
|
| Availability | Will be delivered in 2 to 3 Business Days |
Additional Information
| Alternative name | ALG12 |
| Gene ID | 79087 |
| UniProt | NP_077010 |
| Immunogen | ALG12 (NP_077010, 369 a.a. ~ 426 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 K |
| Isotype | IgG1 kappa |
| Clone | 5E3 |
| Description | Other names: ECM39, MGC111358, MGC3136, PP14673, hALG12asparagine-linked glycosylation 12 homolog (yeast, alpha-1,6-mannosyltransferase) |
| Characteristics | Purified Mouse Monoclonal Antibody (Mab) |
| Specificity | ALG12 (NP_077010, 369 a.a. ~ 426 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
| Molecular Weight | 54655 DA |
| Comments |
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. |
Application Details
| Application Notes | ELISA ~~ 1ug/ml~3ng/ml Western blot ~~ 1:500~1000 |
| Concentration | 1 mg/ml |
| Purification | Purified |
| Buffer | Clear, colorless solution in phosphate buffered saline, pH 7.2 . |
| Storage | Maintain refrigerated at 2-8 deg C for up to 6 months. For long term storage store at -20 deg C in small aliquots to prevent freeze-thaw cycles |
| Research Area | Protein Modifications, Cell Structure |
| Restrictions | For Research Use only |
Images
Publications
| Product |
Jaeken: "Congenital disorders of glycosylation (CDG): update and new developments." in: Journal of inherited metabolic disease, Vol. 27, Issue 3, pp. 423-6, 2004 (PubMed).
Jaeken, Carchon: "Congenital disorders of glycosylation: a booming chapter of pediatrics." in: Current opinion in pediatrics, Vol. 16, Issue 4, pp. 434-9, 2004 (PubMed). Collins, Wright, Edwards et al.: "A genome annotation-driven approach to cloning the human ORFeome." in: Genome biology, Vol. 5, Issue 10, pp. R84, 2004 (PubMed). Gerhard, Wagner, Feingold et al.: "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." in: Genome research, Vol. 14, Issue 10B, pp. 2121-7, 2004 (PubMed). Wan, Gong, Qin et al.: "Large-scale cDNA transfection screening for genes related to cancer development and progression." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 101, Issue 44, pp. 15724-9, 2004 (PubMed). |




