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ALG2 Rabbit pAb (APR27748N)

CAT: 0882-APR27748N-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0882-APR27748N-01Size:50 µL
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Background
This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man (2) GlcNAc (2) -dolichol diphosphate and Man (1) GlcNAc (2) -dolichol diphosphate to form Man (3) GlcNAc (2) -dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii) . Alternative splicing results in multiple transcript variants.
Overview
We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality ALG2 Rabbit pAb (APR27748N) .
Synonyms
ALG2; CDG1I; CDGIi; CMS14; CMSTA3; NET38; hALPG2; alpha-1; 3/1
Gene ID
85365
UniProt
Q9H553
Cellular Locus
Membrane, Single-pass membrane protein
Dilution
WB 1:500 - 1:2000 IHC 1:50 - 1:200
Form
Liquid
Buffer
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Molecular Weight
Calculated MW: 37kDa/47kDa Observed MW: 47kDa
Storage Conditions
Store at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Gene ID URL
https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=85365
Uniprot URL
https://www.uniprot.org/uniprot/Q9H553
AA Sequence
DVLYPSLNVTSFDSVVPEKLDDLVPKGKKFLLLSINRYERKKNLTLALEALVQLRGRLTSQDWERVHLIVAGGYDERVLENVEHYQELKKMVQQSDLGQYVTFLRSFSDKQKISLLHSCTCVLYTPSNEHFGIVPLEAMYMQCPVIAVNSGGPLESIDHSVTGFLCEPDPVHFSEAIEKFIREPSLKATMGLAGRARVKEKFSPEAFTEQLYRYVTKLLV

UniProtKB · Q9H553

Alpha-1,3/1,6-mannosyltransferase ALG2

ALG2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9H553
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ALG2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.4.1.132, 2.4.1.257
Processing
—
Secondary accessions
A2A2Y0, Q8NBX2, Q8NC39
Protein keywords

Coding sequence diversity

Alternative splicing

Disease

Congenital disorder of glycosylationCongenital myasthenic syndromeDisease variant

Cellular component

Endoplasmic reticulumMembrane

Molecular function

GlycosyltransferaseTransferase

Technical term

Proteomics identificationReference proteome

Domain

TransmembraneTransmembrane helix