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Type 2 Rhizomelic Chondrodysplasia Punctata: Disease Bioinformatics

Research of Type 2 Rhizomelic Chondrodysplasia Punctata has been linked to Chondrodysplasia Punctata, Chondrodysplasia Punctata, Rhizomelic, Neurologic Signs, Failure To Thrive, Developmental Delay (disorder). The study of Type 2 Rhizomelic Chondrodysplasia Punctata has been mentioned in research publications which can be found using our bioinformatics tool below. Type 2 Rhizomelic Chondrodysplasia Punctata has been researched in relation to the Myelination Pathway. This pathway complements our catalog of research reagents for the study of Type 2 Rhizomelic Chondrodysplasia Punctata including antibodies and ELISA kits against GNPAT, CHONDRODYSPLASIA, ALKYLDIHYDROXYACETONE PHOSPHATE SYNTHASE.

Type 2 Rhizomelic Chondrodysplasia Punctata Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Type 2 Rhizomelic Chondrodysplasia Punctata below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 6 products for the study of Type 2 Rhizomelic Chondrodysplasia Punctata that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence from our catalog of antibodies and ELISA kits.

H00008443-B01P
Western Blot: GNPAT Antibody [H00008443-B01P] - Analysis of GNPAT expression in transfected 293T cell line by GNPAT polyclonal antibody.  Lane 1: GNPAT transfected lysate(74.8 KDa). Lane 2: Non-transfected lysate.Immunocytochemistry/Immunofluorescence: GNPAT Antibody [H00008443-B01P] - Analysis of purified antibody to GNPAT on HeLa cell. (antibody concentration 10 ug/ml)

Mouse Polyclonal
Species Human
Applications WB, ICC/IF


Related Genes

Type 2 Rhizomelic Chondrodysplasia Punctata has been researched against:

Related Pathways

Type 2 Rhizomelic Chondrodysplasia Punctata has been linked to:

Related Diseases

Type 2 Rhizomelic Chondrodysplasia Punctata has been studied in relation to diseases such as:

Alternate Names

Type 2 Rhizomelic Chondrodysplasia Punctata is also known as Dihydroxyacetonephosphate Acyltransferase Deficiency, Gnpat Deficiency, Human Dihydroxyacetonephosphate Acyltransferase Deficiency.