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Index Finger Anomaly With Pierre Robin Syndrome: Disease Bioinformatics

Research of Index Finger Anomaly With Pierre Robin Syndrome has been linked to Pierre Robin Syndrome, Cleft Palate, Congenital Hand Deformities, Clinodactyly, Micrognathism. The study of Index Finger Anomaly With Pierre Robin Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Index Finger Anomaly With Pierre Robin Syndrome include Ossification, Bone Maturation. These pathways complement our catalog of research reagents for the study of Index Finger Anomaly With Pierre Robin Syndrome including antibodies and ELISA kits against IMPAD1, F8, CANT1.

Index Finger Anomaly With Pierre Robin 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 Index Finger Anomaly With Pierre Robin Syndrome below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 211 products for the study of Index Finger Anomaly With Pierre Robin Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

AF7028
Western blot shows lysates of Neuro‑2A mouse neuroblastoma cell line and PC‑12 rat adrenal pheochromocytoma cell line. PVDF membrane was probed with 1 µg/mL of Sheep Anti-Mouse Inositol Monophosphatase 3/IMPAD1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF7028) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # <a class=Inositol Monophosphatase 3/IMPAD1 was detected in immersion fixed mouse mesenchymal stem cells differentiated into chondrocytes using Sheep Anti-Mouse/Rat Inositol Monophosphatase 3/IMPAD1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF7028) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Sheep IgG Secondary Antibody (red; Catalog # <A class=NoLineLink href=

Sheep Polyclonal
Species Mouse, Rat
Applications WB, ICC

NB100-91761
Western Blot: Factor VIII Antibody [NB100-91761] - Detection of Factor VIII protein in extracts from human umbilical vein endothelial cells (HUVECs).Immunocytochemistry/Immunofluorescence: Factor VIII Antibody [NB100-91761] - Factor VIII antibody was tested 1:50 in HeLa cells with Dylight 488 (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and Dylight 550 (red). Image objective 40X.

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

4 Publications
NBP1-87081
Western Blot: Calcium Activated Nucleotidase 1/CANT1 Antibody [NBP1-87081] - Lane 1: Marker  [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11.  Lane 2: Human cell line RT-4.  Lane 3: Human cell line U-251MG spImmunohistochemistry-Paraffin: Calcium Activated Nucleotidase 1/CANT1 Antibody [NBP1-87081] - Staining of human prostate.

Rabbit Polyclonal
Species Human
Applications WB, IHC, IHC-P

1 Publication

Related Genes

Index Finger Anomaly With Pierre Robin Syndrome has been researched against:

Related Pathways

Index Finger Anomaly With Pierre Robin Syndrome has been linked to:

Alternate Names

Index Finger Anomaly With Pierre Robin Syndrome is also known as Catel-manzke Syndrome.