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Acheiropodia: Disease Bioinformatics

Acheiropodia (ACHP), also known as Horn-Kolb Syndrome is an autosomal recessive disorder that results in hemimelia; a rare birth defect where infants are born without hands or feet.

Acheiropodia 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 Acheiropodia 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 63 products for the study of Acheiropodia that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Immunocytochemistry/Immunofluorescence: LMBR1 Antibody [NBP1-89276] - Staining of human cell line A-431 shows positivity in cytoplasm.Immunohistochemistry-Paraffin: LMBR1 Antibody [NBP1-89276] - Staining of human duodenum shows strong positivity in smooth muscle cells.

Rabbit Polyclonal
Species Human
Applications ICC/IF, IHC, IHC-P

Western Blot: ZP2 Antibody [NBP2-21053] - Sample (30 ug of whole cell lysate) A: IMR32 7. 5% SDS PAGE gel, diluted at 1:1000.Immunohistochemistry-Paraffin: ZP2 Antibody [NBP2-21053] - Immunohistochemical analysis of paraffin-embedded SCC4 xenograft, using antibody at 1:250 dilution.

Rabbit Polyclonal
Species Human
Applications WB, IHC, IHC-P

Related Genes

Acheiropodia has been researched against:

Related Pathways

Acheiropodia has been linked to:

Related PTMs

Alternate Names

Acheiropodia is also known as Acheiropody.