ALG1 Antibody
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


ALG1 Antibody
Background:
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.NCBI Gene ID:
56052Swiss Prot:
Q9BT22Accession Number:
NP_061982Host:
RabbitReactivity:
HumanImmunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ALG1.Clonality:
PolyclonalConjugation:
UnconjugatedType:
Primary AntibodiesField of Research:
Membrane, Signal TransductionPurification:
Antibody is purified by peptide affinity chromatography method.Positive Control:
NTERA2 Cell LysateConcentration:
Batch dependentBuffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.Modification:
NoneShipping Conditions:
Blue IceStorage Conditions:
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store ALG1 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.Calculated Molecular Weight:
52 kDaApplications Notes:
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 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.Symbol:
ALG1NCBI Official Name:
ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferaseNCBI Organism:
Homo sapiensBackground Reference 01:
Grubenmann, C.E., (2004) Hum. Mol. Genet. 13 (5), 535-542.Other Product Names:
ALG1, HMAT1, HMT-1, HMT1, MT-1, CDG1K, Mat-1, hMat-1Tested Applications:
ELISA, WBProtein ID:
41350216Physical Properties:
Liquid
