Research of Esotropia has been linked to Strabismus, Exotropia, Accommodative Component In Esotropia, Refractive Errors, Diplopia. The study of Esotropia has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Esotropia include Transposition, Reflex, Innervation, Pathogenesis, Localization. These pathways complement our catalog of research reagents for the study of Esotropia including antibodies and ELISA kits against STRABISMUS, APHAKIA, EXO, ASAH1, CAT.
Top Research Reagents
We have 1334 products for the study of Esotropia that can be applied to Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: COX5A Antibody [NBP1-32550] - Various whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with COX5A antibody [N1C3] diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](https://images.novusbio.com/fullsize/COX5A-Antibody-Western-Blot-NBP1-32550-img0016.jpg)
![Immunocytochemistry/Immunofluorescence: COX5A Antibody [NBP1-32550] - A431.](https://images.novusbio.com/fullsize/COX5A-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-32550-img0008.jpg)
![Western Blot: GPSM2 Antibody [NBP1-53125] - Sample Tissue: Human Lung Tumor Antibody Dilution: 1.0 ug/ml](https://images.novusbio.com/fullsize/GPSM2-Antibody-Western-Blot-NBP1-53125-img0012.jpg)
![Immunocytochemistry/Immunofluorescence: GPSM2 Antibody [NBP1-53125] - Human cell lines.](https://images.novusbio.com/fullsize/GPSM2-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-53125-img0009.jpg)
![Western Blot: ARC/ARG3.1 Antibody [NBP1-56929] - Reccomended Titration: 0.2 - 1 ug/ml ELISA Titer: 1:312500 Positive Control: Transfected 293T](https://images.novusbio.com/fullsize/ARC-ARG3.1-Antibody-Western-Blot-NBP1-56929-img0010.jpg)
![Immunohistochemistry-Paraffin: ARC/ARG3.1 Antibody [NBP1-56929] - Human adrenal tissue at an antibody concentration of 5ug/ml.](https://images.novusbio.com/fullsize/ARC-ARG3.1-Antibody-Immunohistochemistry-Paraffin-NBP1-56929-img0004.jpg)
![Immunohistochemistry-Paraffin: CRAT Antibody [NBP1-86616] - Analysis in human testis and lymph node tissues. Corresponding CRAT RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/CRAT-Antibody-Immunohistochemistry-Paraffin-NBP1-86616-img0014.jpg)
![Western Blot: CRAT Antibody [NBP1-86616] - Analysis using Anti-CRAT antibody NBP1-86616 (A) shows similar pattern to independent antibody NBP1-86615 (B).](https://images.novusbio.com/fullsize/CRAT-Antibody-Western-Blot-NBP1-86616-img0011.jpg)
![Western Blot: ASAH1 Antibody [NBP1-89296] - Analysis in human cell lines SK-MEL-30 and U-251MG using anti-ASAH1 antibody. Corresponding ASAH1 RNA-seq data are presented for the same cell lines. Loading control: anti-HDAC1.](https://images.novusbio.com/fullsize/ASAH1-Antibody-Western-Blot-NBP1-89296-img0020.jpg)
![Immunohistochemistry-Paraffin: ASAH1 Antibody [NBP1-89296] - Staining of human prostate shows strong granular cytoplasmic positivity in glandular cells.](https://images.novusbio.com/fullsize/ASAH1-Antibody-Immunohistochemistry-Paraffin-NBP1-89296-img0018.jpg)
![Western Blot: gamma-Synuclein Antibody [NBP1-89996] - Lane 1: Marker [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11. Lane 2: Human cell line RT-4](https://images.novusbio.com/fullsize/gamma-Synuclein-Antibody-Western-Blot-NBP1-89996-img0005.jpg)
![Immunohistochemistry-Paraffin: gamma-Synuclein Antibody [NBP1-89996] - Staining of human urinary bladder shows strong cytoplasmic positivity in urothelial cells.](https://images.novusbio.com/fullsize/gamma-Synuclein-Antibody-Immunohistochemistry-Paraffin-NBP1-89996-img0012.jpg)
![Immunocytochemistry/Immunofluorescence: ARC/NOL3 Antibody [NBP2-19561] - Confocal immunofluorescence analysis (Olympus FV10i) of paraformaldehyde-fixed HeLa, using NOL3 antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with (Red) at 1:2000.](https://images.novusbio.com/fullsize/ARC-NOL3-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-19561-img0005.jpg)
![Immunohistochemistry-Paraffin: ARC/NOL3 Antibody [NBP2-19561] - Mouse brain. NOL3 stained by NOL3 antibody diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](https://images.novusbio.com/fullsize/ARC-NOL3-Antibody-Immunohistochemistry-Paraffin-NBP2-19561-img0011.jpg)
![Western Blot: GLYAT Antibody [NBP2-58917] - Western blot analysis in human cell line RT-4, human cell line U-251 MG, human plasma and human liver tissue.](https://images.novusbio.com/fullsize/GLYAT-Antibody-Western-Blot-NBP2-58917-img0002.jpg)
![Immunohistochemistry-Paraffin: GLYAT Antibody [NBP2-58917] - Staining of human skeletal muscle.](https://images.novusbio.com/fullsize/GLYAT-Antibody-Immunohistochemistry-Paraffin-NBP2-58917-img0010.jpg)
![Western Blot: ERG Antibody [NBP2-60655] - Total protein from Human THP-1, Jurkat and K562 cells was separated on a 7.5% 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-ERG in blocking buffer and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.](https://images.novusbio.com/fullsize/ERG-Antibody-Western-Blot-NBP2-60655-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: ERG Antibody [NBP2-60655] - HeLa cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X TBS + 0.5% Triton-X100. The cells were incubated with anti-ERG at 5 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:500 dilution. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse Dylight 550 (Red) at a 1:500 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.](https://images.novusbio.com/fullsize/ERG-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-60655-img0001.jpg)
![Western Blot: Tyrosinase Antibody (JA52-11) [NBP2-67232] - Western blot analysis of Tyrosinase on B16F1 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.](https://images.novusbio.com/fullsize/Tyrosinase-Antibody-JA52-11-Western-Blot-NBP2-67232-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: Tyrosinase Antibody (JA52-11) [NBP2-67232] - Staining Tyrosinase in B16F1 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](https://images.novusbio.com/fullsize/Tyrosinase-Antibody-JA52-11-Immunocytochemistry-Immunofluorescence-NBP2-67232-img0005.jpg)
![Western Blot: CHN 1 Antibody (OTI2G6) - Azide and BSA Free [NBP2-70411] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CHN 1.](https://images.novusbio.com/fullsize/CHN-1-Antibody-OTI2G6-Azide-and-BSA-Free-Western-Blot-NBP2-70411-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: CHN 1 Antibody (OTI2G6) - Azide and BSA Free [NBP2-70411] - Analysis of COS7 cells transiently transfected by pCMV6-ENTRY CHN 1.](https://images.novusbio.com/fullsize/CHN-1-Antibody-OTI2G6-Azide-and-BSA-Free-Immunocytochemistry-Immunofluorescence-NBP2-70411-img0002.jpg)
![Western Blot: Kv11.1 Antibody [NBP3-03109] - Analysis of extracts of various cell lines, using Kv11.1 antibody at 1:500 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 Enhan](https://images.novusbio.com/fullsize/Kv11.1-Antibody-Western-Blot-NBP3-03109-img0004.jpg)
![Immunohistochemistry-Paraffin: Kv11.1 Antibody [NBP3-03109] - Human lung cancer using KCNH2 antibody at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](https://images.novusbio.com/fullsize/Kv11.1-Antibody-Immunohistochemistry-Paraffin-NBP3-03109-img0003.jpg)
![Western Blot: MID1 Antibody [NBP3-05061] - analysis of extracts of HeLa cells, using MID1 Rabbit pAb 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: 60s.](https://images.novusbio.com/fullsize/MID1-Antibody-Western-Blot-NBP3-05061-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: MID1 Antibody [NBP3-05061] - Analysis of MCF-7 cells using MID1 antibody . Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/MID1-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05061-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: SQLE Antibody [NBP2-93808] - Analysis of NIH-3T3 cells using SQLE . Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/SQLE-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-93808-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: SQLE Antibody [NBP2-93808] - Analysis of HeLa cells using SQLE . Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/SQLE-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-93808-img0001.jpg)
