DPAGT1 Antibody

Code CSB-PA884460XA01HU
Size Enquire
Have Questions? Leave a Message or Start an on-line Chat

Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) DPAGT1 Polyclonal antibody
Uniprot No.
Target Names
DPAGT1
Alternative Names
ALG7 antibody; AU021132 antibody; CDG Ij antibody; CDG1J antibody; CMS13 antibody; CMSTA2 antibody; D11S366 antibody; DGPT antibody; Dolichyl phosphate (UDP N acetylglucosamine) acetylglucosaminephosphotransferase 1 (GlcNAc 1 P transferase) antibody; Dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 antibody; DPAGT1 antibody; DPAGT2 antibody; G1PT antibody; GlcNAc 1 P transferase 1 antibody; GlcNAc-1-P transferase antibody; Gnpta antibody; GPT antibody; GPT_HUMAN antibody; H2afx antibody; N-acetylglucosamine-1-phosphate transferase antibody; UAGT antibody; UDP GlcNAc:dolichyl phosphate N acetylglucosaminephosphotransferase antibody; UDP N acetylglucosamine dolichyl phosphate N acetylglucosaminephosphotransferase 1 antibody; UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase antibody; UGAT antibody
Raised in
Rabbit
Species Reactivity
Homo sapiens (Human)
Immunogen
Recombinant Homo sapiens (Human) DPAGT1 protein
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, WB (ensure identification of antigen)
Protocols
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Value-added Deliverables
① 200ug * antigen (positive control);
② 1ml * Pre-immune serum (negative control);
Quality Guarantee
① Antibody purity can be guaranteed above 90% by SDS-PAGE detection;
② ELISA titer can be guaranteed 1: 64,000;
③ WB validation with antigen can be guaranteed positive;
Lead Time
Made-to-order (14-16 weeks)

Customer Reviews and Q&A

 Customer Reviews

There are currently no reviews for this product.

Submit a Review here

Target Background

Function
Catalyzes the initial step of dolichol-linked oligosaccharide biosynthesis in N-linked protein glycosylation pathway: transfers GlcNAc-1-P from UDP-GlcNAc onto the carrier lipid dolichyl phosphate (P-dolichol), yielding GlcNAc-P-P-dolichol.
Gene References into Functions
  1. present work improves our knowledge of DPAGT1-CDG and provides bases for developing tailored splicing and folding therapies PMID: 28662078
  2. Data suggest that N-acetylglucosaminyl 1-phosphate transferase is a breast cancer therapeutic target. PMID: 25408354
  3. Studies show that cells coordinate DPAGT1 expression and protein N-glycosylation with canonical Wnt signaling and E-cadherin adhesion via positive and negative feedback mechanisms. PMID: 23178939
  4. prominent limb-girdle weakness and minimal craniobulbar symptoms who harbour a novel mutation in DPAGT1 PMID: 23591138
  5. Patients with DPAGT1 CMS share similar clinical features with patients who have CMS caused by mutations in GFPT1, another recently identified CMS subtype. PMID: 23447650
  6. Results indicate that the clinical spectrum of dolichyl-phosphate alpha-N-acetylglucosaminyltransferase (DPAGT1)-congenital disorders of glycosylation (CDG) is much broader than appreciated so far. PMID: 23249953
  7. Data suggest that in oral squamous cell carcinoma (OSCC), dysregulation of canonical Wnt signaling and DPAGT1-dependent N-glycosylation induces CTHRC1, thereby driving OSCC cell migration and tumor spread. PMID: 23703614
  8. suggest that the primary pathogenic mechanism of DPAGT1-associated CMS is reduced levels of AChRs at the endplate region. This finding demonstrates that impairment of the N-linked glycosylation pathway can lead to the development of CMS PMID: 23278575
  9. Overexpression of DPAGT1 in human oral squamous cell carcinoma specimens is linked to aberrant activation of canonical Wnt signaling. PMID: 22341307
  10. We identify DPAGT1 as a gene in which mutations cause a congenital myasthenic syndrome. PMID: 22742743
  11. Mutations in DPAGT1 gene is associated with Congenital disorder of glycosylation type Ij. PMID: 22304930
  12. up-regulation of DPAGT1 transcripts by Wnt3a led to altered N-glycosylation of E-cadherin. PMID: 20693288
  13. REVIEW: Structure, expression, and regulation PMID: 19519349
  14. Studies show for the first time that DPAGT1 is an upstream regulator of E-cadherin N-glycosylation status and adherens junction composition and suggest that dysregulation of DPAGT1 causes disturbances in intercellular adhesion in oral cancer. PMID: 19549906

Show More

Hide All

Involvement in disease
Congenital disorder of glycosylation 1J (CDG1J); Myasthenic syndrome, congenital, 13 (CMS13)
Subcellular Location
Endoplasmic reticulum membrane; Multi-pass membrane protein.
Protein Families
Glycosyltransferase 4 family
Database Links

HGNC: 2995

OMIM: 191350

KEGG: hsa:1798

STRING: 9606.ENSP00000346142

UniGene: Hs.524081

icon of phone
Call us
301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
icon of address
Address
7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
icon of social media
Join us with

Subscribe newsletter

Leave a message

* To protect against spam, please pass the CAPTCHA test below.
CAPTCHA verification
© 2007-2024 CUSABIO TECHNOLOGY LLC All rights reserved. 鄂ICP备15011166号-1