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Rabbit Anti-ALG1 Antibody (CSB-PA887118ESR2HU)
Supplier: CUSABIO BIOTECH CO.
Asparagine-linked glycosylation protein 1 homolog;Beta-1 Antibody,4-mannosyltransferase;GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase;GDP-mannose-dolichol diphosphochitobiose mannosyltransferase;Mannosyltransferase-1;MT-1;hMat-1;ALG1;HMAT1 Antibody,HMT1 AntibodyMore alternative names for the antibody
4-mannosyltransferase antibody|Alg1 antibody|ALG1_HUMAN antibody|asparagine-linked glycosylation 1 homolog (yeast, beta-1,4-mannosyltransferase) antibody|asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog (S. cerevisiae) antibody|Asparagine-linked glycosylation protein 1 homolog antibody|Beta 1 4 mannosyltransferase antibody|Beta-1 antibody|CDG1K antibody|Chitobiosyldiphosphodolichol beta-mannosyltransferase antibody|GDP Man GlcNAc2 PP dolichol mannosyltransferase antibody|GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase antibody|GDP-mannose-dolichol diphosphochitobiose mannosyltransferase antibody|Hmat-1 antibody|HMAT1 antibody|HMT 1 antibody|HMT1 antibody|Mannosyltransferase 1 antibody|Mannosyltransferase-1 antibody|MT 1 antibody|MT-1 antibody|MT1 antibody
Anti-ALG1 antibody (ab81134)
Anti-ALG1 antibody (ab81134)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Chitobiosyldiphosphodolichol beta-mannosyltransferase protein (215-464AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:56052( Human), Entrez Gene:208211( Mouse), Entrez Gene:852407( Saccharomyces cerevisiae), Omim:605907( Human), SwissProt:Q9BT22( Human), SwissProt:Q921Q3( Mouse), SwissProt:P16661( Saccharomyces cerevisiae), Unigene:592086( Human), Unigene:34581( Mouse)
|Protein function|| |
Participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. Involved in assembling the dolichol-pyrophosphate-GlcNAc(2)-Man(5) intermediate on the cytoplasmic surface of the ER. .
|Involvement in disease|| |
Congenital disorder of glycosylation 1K (CDG1K) [MIM:608540]: A form of congenital disorder of glycosylation, a multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the glycosyltransferase group 1 family. Glycosyltransferase 33 subfamily.
|Protein cellular localization|| |
Endoplasmic reticulum membrane ; Single-pass type II membrane protein .
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CUSABIO BIOTECH CO.
|Product type|| |
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