Sign in or Register   Sign in or Register
  |  

Mouse Anti-GNPAT Recombinant Antibody (2E5C10) (CBMAB-AP2569LY)

Summary

Host Animal
Mouse
Specificity
Human
Clone
2E5C10
Antibody Isotype
IgG2b
Application
ELISA, WB

Basic Information

Immunogen
Fusion Protein of GNPAT
Specificity
Human
Antibody Isotype
IgG2b
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Glyceronephosphate O-Acyltransferase
Introduction
This gene encodes an enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in this gene are associated with rhizomelic chondrodysplasia punctata. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
Entrez Gene ID
UniProt ID
Alternative Names
Glyceronephosphate O-Acyltransferase; Glycerone-Phosphate O-Acyltransferase; Acyl-CoA:Dihydroxyacetonephosphateacyltransferase; Dihydroxyacetone Phosphate Acyltransferase; EC 2.3.1.42; DHAP-AT;
Function
Dihydroxyacetonephosphate acyltransferase involved in plasmalogen biosynthesis.
Biological Process
Cerebellum morphogenesis Source: Ensembl
Ether lipid biosynthetic process Source: UniProtKB
Fatty acid metabolic process Source: GO_Central
Membrane organization Source: Ensembl
Paranodal junction assembly Source: Ensembl
Phosphatidic acid biosynthetic process Source: Reactome
Phospholipid biosynthetic process Source: GO_Central
Response to drug Source: Ensembl
Response to fatty acid Source: Ensembl
Response to nutrient Source: Ensembl
Response to starvation Source: Ensembl
Synapse assembly Source: Ensembl
Cellular Location
Peroxisome membrane. Exclusively localized to the lumenal side of the peroxisomal membrane.
Involvement in disease
Rhizomelic chondrodysplasia punctata 2 (RCDP2):
A form of rhizomelic chondrodysplasia punctata, a disease characterized by severely disturbed endochondral bone formation, rhizomelic shortening of femur and humerus, vertebral disorders, dwarfism, cataract, cutaneous lesions, facial dysmorphism, and severe mental retardation with spasticity.
Ask a question We look forward to hearing from you.
0 reviews or Q&As
Loading...
Have you used Mouse Anti-GNPAT Recombinant Antibody (2E5C10)?
Submit a review and get a Coupon or an Amazon gift card. 20% off Coupon $30 eGift Card
Submit a review
Loading...
For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

Online Inquiry

Documents

Contact us

  • Tel: (USA)
  • (UK)
  • Fax:
  • Email:

Submit A Review

Go to
Compare