ALG1 anticorps
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- Antigène Voir toutes ALG1 Anticorps
- ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp ALG1 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by peptide affinity chromatography method.
- Immunogène
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ALG1.
- Top Product
- Discover our top product ALG1 Anticorps primaire
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- Indications d'application
- ALG1 antibody can be used for detection of ALG1 by ELISA at 1:62500. ALG1 antibody can be used for detection of ALG1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Conseil sur la manipulation
- As with any antibody avoid repeat freeze-thaw cycles.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store ALG1 antibody at -20 °C.
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- Antigène
- ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))
- Autre désignation
- ALG1 (ALG1 Produits)
- Synonymes
- anticorps CDG1K, anticorps HMAT1, anticorps HMT-1, anticorps HMT1, anticorps MT-1, anticorps Mat-1, anticorps hMat-1, anticorps zgc:66221, anticorps wu:fi34b12, anticorps alg1, anticorps hmat1, anticorps hmt1, anticorps ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase, anticorps asparagine-linked glycosylation 1 (beta-1,4-mannosyltransferase), anticorps Beta-mannosyltransferase, anticorps ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase L homeolog, anticorps ALG1, anticorps Alg1, anticorps alg1, anticorps alg1.L
- Sujet
- ALG1 catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. Defects in ALG1 are the cause of congenital disorder of glycosylation type 1K (CDG1K).The biosynthesis of lipid-linked oligosaccharides is highly conserved among eukaryotes and is catalyzed by 14 glycosyltransferases in an ordered stepwise manner. Mannosyltransferase I (MT I) catalyzes the first mannosylation step in this process.
- Poids moléculaire
- 52 kDa
- ID gène
- 56052
- NCBI Accession
- NP_061982
- UniProt
- Q9BT22
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