GNPAT Antibodies

AND GNPAT ELISA kits, GNPAT Proteins

Many biological assays use antibodies to detect GNPAT, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with GNPAT in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop GNPAT antibodies...

We validate the specificity of these antibodies to GNPAT by testing them on tissues known to express GNPAT positively and negatively. Browse below to find the GNPAT antibody that suites your experiment. We have 3 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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GNPAT Infographic by Boster Bio

All GNPAT Products

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Product

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Specificity

Applications

Price

Anti-GNPAT (F365) Antibody

Human, Mouse, Rat

IHC, WB

$405
Cat # A07205
100ul

Anti-GNPAT Mouse Monoclonal Antibody [Clone ID: OTI1E7]

Human

IHC, WB

$523
Cat # M07205
100 µl

GNPAT (NM_014236) Human Over-expression Lysate

Human

$628
Cat # LS008443
100 µg

GNPAT Overview

Facts about Dihydroxyacetone phosphate acyltransferase.

GNPAT 3D structure. Source: alphafold

Dihydroxyacetone phosphate acyltransferase (GNPAT)

Gene Information

Human
Gene Name:	GNPAT
Uniprot:	O15228
Entrez:	8443

Family

Belongs to:

GPAT/DAPAT family

Alternative Names

Acyl-CoA:dihydroxyacetonephosphateacyltransferase; DAPATdihydroxyacetone phosphate acyltransferase; DHAP-AT; DHAPATDAP-ATacyl-CoA:dihydroxyacetonephosphateacyltransferase; EC 2.3.1; EC 2.3.1.42; Glycerone-phosphate O-acyltransferase; glyceronephosphate O-acyltransferase

Molecular Weight

Mass (kDA):
77.188 kDA

Genomic Context


Human

Location:	1q42.2
Sequence:	1; NC_000001.11 (231241210..231277973)

Subcellular Localizations

Peroxisome membrane; Peripheral membrane protein; Matrix side. Exclusively localized to the lumenal side of the peroxisomal membrane.

Diseases

Chondrodysplasia Punctata, Rhizomelic
Chondrodysplasia Punctata
Bilateral Cataracts (disorder)
Limb Deformities, Congenital
Profound Mental Retardation
Metastatic Melanoma
Melanoma
Schizophrenia
Skeletal Dysplasia
Dysplasia
Neoplasms

Kidney Diseases
Chronic Kidney Disease
Inflammation
Congenital Hand Deformities
Type 2 Rhizomelic Chondrodysplasia Punctata
Uniparental Disomy

PTMs

Phosphorylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/GNPAT

References

PMID: 9459311 by Thai T.-P., et al. Ether lipid biosynthesis: isolation and molecular characterization of human dihydroxyacetonephosphate acyltransferase.

PMID: 9536089 by Ofman R., et al. Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2.