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MGAT2 Rabbit Polyclonal Antibody (HRP)

CAT: 0013-GTR18376555Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18376555Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
MGAT2 Rabbit Polyclonal Antibody (HRP)
Product Name Alternative
GNT2, CDG2A, CDGS2, GNT-II, GLCNACTII
UniProt
Q10469
Immunogen
The immunogen is a synthetic peptide directed towards the middle region of human MGAT2
Clonality
Polyclonal
Conjugation
HRP
Sequence
Synthetic peptide located within the following region: YAGLILFLEEDHYLAPDFYHVFKKMWKLKQQECPECDVLSLGTYSASRSF
Field of Research
Signal Transduction
Purification
Affinity Purified
Form
Liquid. Purified antibody is supplied in high phosphate PBS, 100 mm phosphate, 150 mM NaCl, pH 7.6.
Molecular Weight
51kDa
Storage Conditions
All conjugated antibodies should be stored in light-protected vials or covered with a light protecting material (i.e. aluminum foil) . Conjugated antibodies are stable for at least 12 months at 4C. If longer storage is desired (24 months), conjugates may be diluted with up to 50% glycerol and stored at -2°C to -8°C. Freezing and thawing conjugated antibodies will compromise enzyme activity as well as antibody binding.
Notes
For research use only.
Prediction Reactivity
Bovine, Canine, Equine, Guinea pig, Human, Mouse, Porcine, Rabbit, Rat, Zebrafish
Tested Applications
WB
NCBI Accession Number
NP_002399
Host or Source
Rabbit
Preservative
Liquid. Purified antibody is supplied in high phosphate PBS, 100 mm phosphate, 150 mM NaCl, pH 7.6.

UniProtKB · Q10469

Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase

MGAT2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q10469
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
MGAT2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.4.1.143
Processing
—
Secondary accessions
B3KPC5, B3KQM0
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Disease

Congenital disorder of glycosylationDisease variant

PTM

Disulfide bondGlycoprotein

Molecular function

GlycosyltransferaseTransferase

Cellular component

Golgi apparatusMembrane

Ligand

ManganeseMetal-binding

Domain

Signal-anchorTransmembraneTransmembrane helix

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