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Sacral Meningocele Conotruncal Heart Defects: Disease Bioinformatics

Research of Sacral Meningocele Conotruncal Heart Defects has been linked to Congenital Heart Defects, Meningomyelocele, Digeorge Syndrome, Hydrocephalus, Ventricular Septal Defects. The study of Sacral Meningocele Conotruncal Heart Defects has been mentioned in research publications which can be found using our bioinformatics tool below. Sacral Meningocele Conotruncal Heart Defects has been researched in relation to the Transposition Pathway. This pathway complements our catalog of research reagents for the study of Sacral Meningocele Conotruncal Heart Defects including antibodies and ELISA kits against CTCFL, TBX1, CITED2.

Sacral Meningocele Conotruncal Heart Defects 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 Sacral Meningocele Conotruncal Heart Defects 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 89 products for the study of Sacral Meningocele Conotruncal Heart Defects that can be applied to Chromatin Immunoprecipitation, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP2-52405
Western Blot: BORIS Antibody (20B11) [NBP2-52405] - Antibody from clone 20B11 specifically recognises the C terminal domain of BORIS, and the endogenous and exogenous BORIS protein. Cell lysates were resolved by SDS-PAGE, blotted and probed with the original mouse supernatant of the 20B11 clone. Positions of BORIS and the C-terminal domain of BORIS are indicated. B, bacterially expressed BORIS;  293T cells transfected with 0.5ug of the plasmid expressing BORIS; M, Molecular marker.Immunohistochemistry: BORIS Antibody (20B11) [NBP2-52405] - Analysis using the supernatants from the clone 20B11 at following dilutions: (A) 20B11 undiluted supernatant and (B) 20B11 at 1:25. (B) Cells have been counterstained with the nuclear marker hematoxylin (blue). Images were taken at x60 magnification using the Olympus BX41 microscope. Expression of BORIS protein is indicated by the presence of brown staining, with a pattern characteristic for BORIS ( both, cytoplasmic and nuclear).

Mouse Monoclonal
Species Human
Applications WB, ChIP, ELISA

1 Publication
NBP2-46076
Western Blot: TBX1 Antibody (1C2) [NBP2-46076] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY TBX1.Immunohistochemistry: TBX1 Antibody (1C2) [NBP2-46076] - Analysis of Human lymph node tissue. (Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)

Mouse monoclonal
Species Human
Applications WB, IHC

NB100-136
Western Blot: Cited-2 Antibody (JA22) [NB100-136] - Total protein from human HeLa and MCF7 and mouse 3T3 cell lines was separated on a 12% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST.  The membrane was probed with 2.0 ug/ml anti-Cited in 1% non-fat milk in TBST and detected with an anti-mouse HRP secondary antibody using West Pico PLUS chemiluminescence detection reagent.Immunocytochemistry/Immunofluorescence: Cited-2 Antibody (JA22) [NB100-136] - The Cited-2 (JA22) antibody was tested at a 1:250 dilution in HeLa cells against Dylight 488 (Green). Beta-tubulin and nuclei were counterstained against Dylight 550 (Red) and DAPI (Blue).

Mouse Monoclonal
Species Human, Mouse
Applications WB, ICC/IF, IHC

12 Publications

Related Genes

Sacral Meningocele Conotruncal Heart Defects has been researched against:

Related Pathways

Sacral Meningocele Conotruncal Heart Defects has been linked to:

Alternate Names

Sacral Meningocele Conotruncal Heart Defects is also known as Kousseff Syndrome.