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Eem Syndrome: Disease Bioinformatics

Research of Eem Syndrome has been linked to Dystrophy, Ectodermal Dysplasia, Ectrodactyly, Dysplasia, Age Related Macular Degeneration. The study of Eem Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Eem Syndrome include Pigmentation, Hair Follicle Morphogenesis, Limb Development. These pathways complement our catalog of research reagents for the study of Eem Syndrome including antibodies and ELISA kits against P-CADHERIN, CDH3, CDH15, RPE65, UVRAG.

Eem Syndrome 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 Eem Syndrome 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 119 products for the study of Eem Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Western Blot: P-Cadherin Antibody (2D5) [NBP2-45601] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY P-Cadherin.Immunohistochemistry: P-Cadherin Antibody (2D5) [NBP2-45601] - Analysis of Human lymph node tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)

Mouse monoclonal
Species Human
Applications WB, IHC, IF

Other p63/TP73L Recombinant Protein

Species Human
Applications WB, ELISA, PA

1 Publication
Immunohistochemistry: M-Cadherin/Cadherin-15 Antibody [NBP1-88101] - Immunohistochemical staining of human smooth muscle shows strong cytoplasmic positivity in smooth muscle cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

Western Blot: CKAP4 Antibody [NBP1-26642] - Whole cell lysate from HeLa, 293T and mouse NIH3T3 cells. CKAP4 was also immunoprecipitated by rabbit anti-CKAP4 antibodies NBP1-26641and NBP1-26643.Immunocytochemistry: CKAP4/p63 Antibody [NBP1-26642] - FFPE section of human placenta.  Antibody used at a dilution of 1:500. Detection: DAB staining using Immunohistochemistry Accessory Kit.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, ICC/IF, IHC

1 Publication
Western Blot: RPE65 Antibody (401.8B11.3D9) [NB100-355] - WB analysis of RPE65 in 20ug lysate of COS7 cells expressing recombinant Human RPE65 (Lane 1) and 5ug of Bovine retinal pigment epithelium membrane fraction (Lane 2). Blot processed for detection with alkaline phosphatase conjugated goat-anti Mouse IgG secondary antibody and NBT/BCIP substrate. Immunocytochemistry/Immunofluorescence: RPE65 Antibody (401.8B11.3D9) [NB100-355] - ICC-IF analysis of cultured ARPE19 cells, a spontaneously arising human retinal pigment epithelia cell line - 10 minutes fixation in 4% PFA, 10 minutes permeabilization in PBS containing 0.2% Triton X-100 (PBS-T), 1 hour blocking in 10% normal goat serum containing 1% BSA in PBS-T, 1:100 primary antibody dilution in PBS, ON 4C incubation.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, Flow, ICC/IF

     5 Reviews

35 Publications
Immunohistochemistry-Paraffin: ELSPBP1 Antibody [NBP2-13957] - Staining of human epididymis shows strong cytoplasmic positivity in glandular cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

Western Blot: UVRAG Antibody [NBP2-24482] - Analysis of UVRAG in human heart lysate in the 1) absence and 2) presence of immunizing peptide, 3) mouse heart and 4) rat heart using this antibody at 0 ug/ml, 0.5 ug/ml and 0.5 ug/ml, respectively.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB

Related Genes

Eem Syndrome has been researched against:

Related Pathways

Eem Syndrome has been linked to:

Related PTMs

Alternate Names

Eem Syndrome is also known as eem syndrome, ectodermal dysplasia, ectrodactyly, and macular dystrophy, ectodermal dysplasia.