1-832-868-1888
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Catalog Number: |
25355 |
| other_names: | DPAGT, DGPT, GPT, ALG7, G1PT, UAGT, UGAT, CDG1J, CDG-Ij, UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase |
Amount: |
100μg |
| calculated_mw: | |
| host_species: | Rabbit |
Price: |
$319 |
Swiss-Prot No: |
Swiss-Prot:Q9H3H5 |
Form of Antibody: |
Supplied in PBS containing 0.02% sodium azide. |
Storage/Stability: |
|
Immunogen: |
Raised against a 17 amino acid peptide near the amino terminus of human DPAGT1. |
Purification: |
Affinity chromatography purified via peptide column |
Specificity/Sensitivity: |
At least four isoforms of DPAGT1 are known to exist; this antibody will recognize the two longest isoforms. DPAGT1 antibody is predicted to not cross-react with UHRF1BP1. |
Applications: |
ELISA WB |
Background: |
The UDP-N-acetylglucosamine-dolichyl-phosphate N-acetyl-glucosaminephosphotransferase (DPAGT1) is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway for glycoprotein biosynthesis. Mutations in this integral endoplasmic reticulum (ER) membrane protein enzyme belongs to the glycosyltransferase family 4 results in the congenital disorder of glycosylation type Ij with symptoms such as severe hypotonia, medically intractable seizures, mental retardation, microcephaly, and exotropia. Recent experiments have shown that DPAGT1 is a target of the Wnt/beta-catenin signaling pathway, with Wnt3a inducing higher DPAGT1 mRNA expression. |
References: |
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appl_detail: |
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