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Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form: Disease Bioinformatics

Research of Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form has been linked to Bulla, Epidermolysis Bullosa, Epidermolysis Bullosa Dystrophica, Skin Diseases, Vesiculobullous, Cicatrix. The study of Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form include Transport, Phagocytosis, Pathogenesis, Excretion, Secretion. These pathways complement our catalog of research reagents for the study of Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form including antibodies and ELISA kits against COL7A1, PLOD1, DST, IK.

Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form 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 Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form 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 31 products for the study of Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP2-37900
Immunohistochemistry-Paraffin: Collagen VII Antibody [NBP2-37900] - Staining of human liver shows no positivity in hepatocytes as expected.Immunohistochemistry-Paraffin: Collagen VII Antibody [NBP2-37900] - Staining of human skin shows moderate membranous positivity in epidermal cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NBP2-38770
Western Blot: PLOD1 Antibody [NBP2-38770] - Analysis in human cell line U-87 MG.Western Blot: PLOD1 Antibody [NBP2-38770] - SC65 directly interacts with lysyl-hydroxylase 1 (LH1). Western blot of primary calvarial osteoblast and skin fibroblast lysates from WT and Sc65KO 3 day-old mice (N = 2) showing significantly decreased levels of LH1 protein in Sc65KO samples. Densitometric quantification of LH1 protein normalized to beta-actin from the western blot shown above (*p<0.05; error bars represent SD). All experiments were performed at least 3 times.  Image collected and cropped by CiteAb from the following publication (http://dx.plos.org/10.1371/journal.pgen.1006002), licensed under a CC-BY licence.

Rabbit Polyclonal
Species Human, Mouse
Applications WB

2 Publications
NBP1-89946
Immunocytochemistry/Immunofluorescence: Dystonin Antibody [NBP1-89946] - Staining of human cell line A-431 shows localization to nucleus & cytosol. Antibody staining is shown in green.Immunohistochemistry-Paraffin: Dystonin Antibody [NBP1-89946] - Staining of human tonsil shows low positivity in non-germinal center cells as expected.

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

NBP1-30927
Western Blot: RED Antibody [NBP1-30927] - Sample (30 ug of whole cell lysate) A: THP-1 B: HL-60 7. 5% SDS PAGE; antibody diluted at 1:1000.Immunocytochemistry/Immunofluorescence: RED Antibody [NBP1-30927] - Analysis of HeLa, using NBP1-30927 at 1:200 dilution.

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


Related Genes

Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form has been researched against:

Related Pathways

Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form has been linked to:

Related PTMs

Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form is also known as Transient Bullous Dermolysis Of The Newborn.