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Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis And Hypoplastic Teeth: Disease Bioinformatics

Mental Retardation, Congenital Heart Disease, Blepharophimosis, and Hypoplastic Teeth have all been linked in several cases. Congenital Heart Disease is when there are problems with the heart at birth. Blepharophimosis is when the eye lids are shortened and the nasal bridge is flattened. Hypoplastic Teeth is when there is reduced enamel on the teeth. These conditions have been linked to mental retardation and are still being studied.

Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis And Hypoplastic Teeth 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 Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis And Hypoplastic Teeth below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 166 products for the study of Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis And Hypoplastic Teeth that can be applied to Chromatin Immunoprecipitation, Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NB100-1277
Western Blot: FOXL2 Antibody [NB100-1277] - Staining of K562 cell lysate (A) + peptide (B) and HeLa cell lysate (C) + peptide (D) 35 ug protein in RIPA buffer). FOXL2 antibody at 2 ug/mL. Detected by chemiluminescence.Immunocytochemistry/Immunofluorescence: FOXL2 Antibody [NB100-1277] - Analysis of FOXL2 in PFA-fixed, E14.5 mouse ovary section using anti-FOXL2 antibody (magenta), germ cell marker (green) and hoechst (grey). ICC/IF image submitted by a verified customer review.

Goat Polyclonal
Species Human, Mouse, Ferret
Applications WB, ChIP, ICC/IF

     1 Review

40 Publications
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
NBP1-30475
Western Blot: BRD2 Antibody [NBP1-30475] - Detection of Human and Mouse BRD2 by Western Blot. Samples: Whole cell lysate (50 ug) from HeLa, 293T, and mouse NIH3T3 cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-BRD2 antibody NBP1-30475 used for WB at 0.04 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.Immunocytochemistry/Immunofluorescence: BRD2 Antibody [NBP1-30475] - Formaldehyde-fixed asynchronous HeLa cells. Antibody: Affinity purified rabbit anti- BRD2 used at a dilution of 1:100 (2ug/ml) (left) and rabbit anti-BRD2 recombinant monoclonal used at a dilution of 1:20 (right). Detection: Red-fluorescent goat anti-rabbit IgG cross-adsorbed Antibody DyLight 594 conjugated.

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

1 Publication
MOB00
 Leptin/OB [HRP] Leptin/OB [HRP]


Species Mouse, Rat

     4 Reviews

120 Publications

Related Genes

Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis And Hypoplastic Teeth has been researched against:

Alternate Names

Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis And Hypoplastic Teeth is also known as Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis, And Hypoplastic Teeth, Ohdo Blepharophimosis Syndrome.