Submit your image related to Diseases to be featured!

Get Social

Submit your Twitter account related to Eye Anterior Chamber Congenital Anomaly to be featured!

Blogs

Submit your blog on Eye Anterior Chamber Congenital Anomaly to be featured!

Events

Submit your event on Eye Anterior Chamber Congenital Anomaly to be featured!

Videos

Submit your video on Eye Anterior Chamber Congenital Anomaly to be featured!

Charities

Submit your charity on Eye Anterior Chamber Congenital Anomaly to be featured!

Eye Anterior Chamber Congenital Anomaly: Disease Bioinformatics

Research of Eye Anterior Chamber Congenital Anomaly has been linked to Eye Abnormalities, Intraocular Pressure Disorder, Cleft Palate, Orbital Separation Excessive, Cleft Lip. The study of Eye Anterior Chamber Congenital Anomaly has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Eye Anterior Chamber Congenital Anomaly including antibodies and ELISA kits against SS18L1, INS, IGF1, INPP5K, IRF6.

Eye Anterior Chamber Congenital Anomaly 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 Eye Anterior Chamber Congenital Anomaly 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 692 products for the study of Eye Anterior Chamber Congenital Anomaly that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry, Chromatin Immunoprecipitation (ChIP) from our catalog of antibodies and ELISA kits.

NBP2-20486
Western Blot: SS18L1 Antibody [NBP2-20486] - Sample (50 ug of whole cell lysate) A: Mouse Brain, 10% SDS PAGE gel, diluted at 1:1000.Immunocytochemistry/Immunofluorescence: SS18L1 Antibody [NBP2-20486] - Immunofluorescence analysis of paraformaldehyde-fixed A431, using antibody at 1:500 dilution.

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

NBP2-34260
Immunohistochemistry-Paraffin: Insulin Antibody (E2-E3 (same as INS04)) [NBP2-34260] - Insulin E2E3, human pancreas (FFPE), HIER pH 9 antigen retrieval. Image from verified customer review.Immunohistochemistry-Paraffin: Insulin Antibody (E2-E3 (same as INS04)) [NBP2-34260] - Formalin-fixed, paraffin-embedded human pancreas stained with insulin Monoclonal Antibody (E2-E3)

Mouse Monoclonal
Species Human, Mouse, Porcine
Applications WB, Flow, ICC/IF

     5 Reviews

1 Publication
291-G1
1 μg/lane of Recombinant Human IGF-I/IGF-1 was resolved with SDS-PAGE under reducing (R) conditions and visualized by silver staining, showing a single band at 7 kDa.Recombinant Human IGF-I/IGF-1 (Catalog # 291-G1) stimulates proliferation in the MCF-7 human breast cancer cell line. The ED<sub>50</sub> for this effect is 0.3‑1.5 ng/mL.


Species Human

     5 Reviews

136 Publications
NBP2-94173
Western Blot: SKIP Antibody [NBP2-94173] - Analysis of extracts of various cell lines, using SKIP at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 90s.Immunocytochemistry/Immunofluorescence: SKIP Antibody [NBP2-94173] - Analysis of U2OS cells using SKIP at dilution of 1:100. Blue: DAPI for nuclear staining.

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

NBP1-51911
Western Blot: IRF6 Antibody [NBP1-51911] - HEK293 overexpressing IRF6 and probed with (mock transfection in first lane).Immunohistochemistry-Paraffin: IRF6 Antibody [NBP1-51911] - Staining of paraffin embedded Human Kidney. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.

Goat Polyclonal
Species Human, Mouse
Applications WB, IHC, IHC-P

5 Publications

Related Genes

Eye Anterior Chamber Congenital Anomaly has been researched against:

Alternate Names

Eye Anterior Chamber Congenital Anomaly is also known as Anterior Chamber Anomalies.