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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
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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

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).