Research of Retinal Vein Occlusion has been linked to Venous Occlusion, Central Retinal Vein Occlusion, Edema, Macular Retinal Edema, Venous Retinal Branch Occlusion. The study of Retinal Vein Occlusion has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Retinal Vein Occlusion include Pathogenesis, Coagulation, Angiogenesis, Fibrinolysis, Platelet Aggregation. These pathways complement our catalog of research reagents for the study of Retinal Vein Occlusion including antibodies and ELISA kits against VEGFA, PRH2, TISSUE PLASMINOGEN ACTIVATOR, ERG, KCNH2.
Top Research Reagents
We have 1933 products for the study of Retinal Vein Occlusion that can be applied to Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Knockdown Validated: Calreticulin Antibody [NB600-101] - Western blot shows lysates of HeLa human cervical epithelial carcinoma parental cell line and Calreticulin knockout (KO) HeLa cell line. PVDF membrane was probed with 1:1500 of Rabbit Anti-Human Calreticulin Polyclonal Antibody (Catalog # NB600-101) followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog #HAF008). Specific band was detected for Calreticulin at approximately 55 kDa (as indicated) in the parental HeLa cell line, but is not detectable in the knockout HeLa cell line. This experiment was conducted under reducing conditions.](https://images.novusbio.com/fullsize/Calreticulin-Antibody-Knockdown-Validated-NB600-101-img0011.jpg)
![Western Blot: Calreticulin Antibody [NB600-101] - Human kidney lysate.](https://images.novusbio.com/fullsize/Calreticulin-Antibody-Western-Blot-NB600-101-img0006.jpg)
![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: Coagulation Factor II/Thrombin Antibody [NBP1-58268] - 721_B tissue lysate at a concentration of 1ug/ml.](https://images.novusbio.com/fullsize/Coagulation-Factor-II-Thrombin-Antibody-Western-Blot-NBP1-58268-img0007.jpg)
![Immunohistochemistry: Coagulation Factor II/Thrombin Antibody [NBP1-58268] - Analysis of human liver after heat-induced Antigen retrieval. Antibody concentration 5 ug/ml.](https://images.novusbio.com/fullsize/Coagulation-Factor-II-Thrombin-Antibody-Immunohistochemistry-NBP1-58268-img0008.jpg)
![Western Blot: Frataxin Antibody (1C12) [NBP2-01743] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Frataxin (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-Frataxin.](https://images.novusbio.com/fullsize/Frataxin-Antibody-1C12-Western-Blot-NBP2-01743-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: Frataxin Antibody (1C12) [NBP2-01743] Staining of COS7 cells transiently transfected by pCMV6-ENTRY Frataxin.](https://images.novusbio.com/fullsize/Frataxin-Antibody-1C12-Immunocytochemistry-Immunofluorescence-NBP2-01743-img0009.jpg)
![Western Blot: SLC6A8 Antibody [NBP2-11567] - Mouse Heart lysate (35 ug protein in RIPA buffer). Antibody at 0.1 ug/ml, 1 hr incubation. Detected by chemiluminescence.](https://images.novusbio.com/fullsize/SLC6A8-Antibody-Western-Blot-NBP2-11567-img0002.jpg)
![Immunohistochemistry-Paraffin: SLC6A8 Antibody [NBP2-11567] - Human kidney. Antibody at 5 ug/ml. Steamed antigen retrieval with citrate buffer pH6, AP-staining.](https://images.novusbio.com/fullsize/SLC6A8-Antibody-Immunohistochemistry-Paraffin-NBP2-11567-img0003.jpg)
![Western Blot: MTHFR Antibody (5D3) [NBP2-37607] - Western blot analysis using MTHFR mouse mAb against Rat Heart cell lysate.](https://images.novusbio.com/fullsize/MTHFR-Antibody-5D3-Western-Blot-NBP2-37607-img0003.jpg)
![Immunohistochemistry-Paraffin: MTHFR Antibody (5D3) [NBP2-37607] - Analysis of intima cancer tissues (left) and prostate tissues (right) using MTHFR mouse mAb with DAB staining.](https://images.novusbio.com/fullsize/MTHFR-Antibody-5D3-Immunohistochemistry-Paraffin-NBP2-37607-img0006.jpg)
![Western Blot: FACA/FANCA Antibody [NB100-2564] - Detection of FANC A in transfected COS1 cell lysate.](https://images.novusbio.com/fullsize/FACA-FANCA-Antibody-Western-Blot-NB100-2564-img0004.jpg)
![N/A Serpin F1/PEDF [Biotin]](https://images.novusbio.com/fullsize2/DATA_Serpin_F1_DY117705_ELISA_2344.jpg)
![N/A VEGF [HRP]](https://images.novusbio.com/fullsize2/DATA_VEGF_DVE00_ELISA_871.jpg)
![N/A VEGF [HRP]](https://images.novusbio.com/fullsize2/DATA_VEGF_DVE00_ELISA_872.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: 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)
![SDS-Page: Recombinant Human PRH2 Protein [H00005555-P01] - 12.5% SDS-PAGE Stained with Coomassie Blue.](https://images.novusbio.com/fullsize/qc_test-H00005555-P01-1.jpg)
