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Type I Familial Incomplete Male Pseudohermaphroditism: Disease Bioinformatics

Research of Type I Familial Incomplete Male Pseudohermaphroditism has been linked to Pseudohermaphroditism Male, Disorders Of Sex Development, Gynecomastia, Testicular Feminization, Reifenstein Syndrome. The study of Type I Familial Incomplete Male Pseudohermaphroditism has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Type I Familial Incomplete Male Pseudohermaphroditism including antibodies and ELISA kits against PLOD1, VCAM1, L1CAM, ANDROGEN-BINDING PROTEIN, MECP2.

Type I Familial Incomplete Male Pseudohermaphroditism 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 I Familial Incomplete Male Pseudohermaphroditism 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 491 products for the study of Type I Familial Incomplete Male Pseudohermaphroditism that can be applied to Chromatin Immunoprecipitation, Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

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
DVC00
 VCAM-1/CD106 [HRP] VCAM-1/CD106 [HRP]


Species Human

81 Publications
NB100-2682

Mouse Monoclonal
Species Human, Mouse
Applications WB, ELISA, Flow

1 Publication
NB600-1101
Western Blot: MeCP2 Antibody [NB600-1101] - Analysis of HeLa cell extract.Immunocytochemistry/Immunofluorescence: MeCP2 Antibody [NB600-1101] - Analysis of Methyl CpG Binding Protein 2 (green) showing staining in the nucleus of C2C12 cells (right) compared to a negative control without primary antibody (left).

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

4 Publications

Related Genes

Type I Familial Incomplete Male Pseudohermaphroditism has been researched against:

Alternate Names

Type I Familial Incomplete Male Pseudohermaphroditism is also known as Familial Incomplete Male Pseudohermaphroditism, Type 1, Lubs Syndrome.