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POMGNT2 Rabbit Polyclonal Antibody (APC)

CAT: 0013-GTR18531721Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18531721Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Anti-POMGNT2 Antibody. Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat.
Product Name Alternative
POMGNT2; AGO61; C3orf39; EOGTL; GTDC2; Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2; POMGnT2; Extracellular O-linked N-acetylglucosamine transferase-like; Glycosyltransferase-like domain-containing protein 2
UniProt
Q8NAT1
Reactivity
Human, Mouse, Rat
Immunogen
E.coli-derived human POMGNT2 recombinant protein (Position: R40-K378) . Human POMGNT2 shares 94.7% and 95% amino acid (aa) sequence identity with mouse and rat POMGNT2, respectively.
Target
Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2
Clonality
Polyclonal
Conjugation
APC
Field of Research
Cell Biology
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Storage Conditions
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
IgG

UniProtKB · Q8NAT1

Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2

PMGT2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q8NAT1
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
POMGNT2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
POMGnT2
EC number
2.4.1.312
Processing
—
Secondary accessions
B3KWC3, Q96SY3
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Disease

Congenital muscular dystrophyDisease variantDystroglycanopathyLimb-girdle muscular dystrophyLissencephaly

Cellular component

Endoplasmic reticulumMembrane

PTM

Glycoprotein

Molecular function

GlycosyltransferaseTransferase

Domain

Signal-anchorTransmembraneTransmembrane helix

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