Research of Ocular Cicatricial Pemphigoid has been linked to Bullous Pemphigoid, Pemphigoid, Benign Mucous Membrane, Conjunctival Diseases, Corneal Diseases, Cicatrix. The study of Ocular Cicatricial Pemphigoid has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Ocular Cicatricial Pemphigoid include Pathogenesis, Keratinization, Localization, Secretion, Glycosylation. These pathways complement our catalog of research reagents for the study of Ocular Cicatricial Pemphigoid including antibodies and ELISA kits against LACRIMAL, MUCIN, TGF-BETA1, AMT, DST.
Top Research Reagents
We have 4997 products for the study of Ocular Cicatricial Pemphigoid that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: Ceruloplasmin Antibody (6C3K9) [NBP3-15868] - Analysis of extracts of various cell lines, using Ceruloplasmin antibody (NBP3-15868) at 1:5000 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: 1s.](https://images.novusbio.com/fullsize/Ceruloplasmin-Antibody-6C3K9-Western-Blot-NBP3-15868-img0006.jpg)
![Immunohistochemistry: Ceruloplasmin Antibody (6C3K9) [Ceruloplasmin] - Immunohistochemistry analysis of paraffin-embedded Rat brain tissue using Ceruloplasmin Rabbit mAb at a dilution of 1:10000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.](https://images.novusbio.com/fullsize/nbp3-15868_rabbit-ceruloplasmin-mab-6c3k9-52202517251917.jpg)
![Western Blot: NOD2 Antibody (2D9) [NB100-524] - HCMV infection induces NOD2 mRNA and protein in HFFs and U373 cells. E. U373 glioma cells were infected with HCMV Towne strain and levels of NOD1, NOD2 and GAPDH mRNAs were measured by qRT-PCR at indicated time points. F. HFFs were infected with HCMV (Towne) at MOI of 1 PFU/cell and levels of NOD2 protein and B-actin were determined 48 and 72 hpi. G. HFFs were infected with HCMV (Towne) strain at MOI of 0.03 or 3 PFU/cell and levels of NOD2 protein and B-actin were determined at 48 hpi. Quantitative data represent mean values (+/-SD) of triplicate determinations from three independent experiments (*p<0.05, **p<0.01, ***p<0.001, one-way ANOVA test). Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0092704.g001) licensed under a CC-BY license.](https://images.novusbio.com/fullsize/NOD2-Antibody-2D9-Western-Blot-NB100-524-img0018.jpg)
![Immunohistochemistry-Frozen: NOD2 Antibody (2D9) [NB100-524] - Overlay of NOD2-DyLight 488 (green) with phase contrast of murine colon. Image from verified customer review.](https://images.novusbio.com/fullsize/NOD2-Antibody-2D9-Immunohistochemistry-Frozen-NB100-524-img0016.jpg)
![N/A IL-6 [HRP]](https://images.novusbio.com/fullsize/d6050b_human-il-6-quantikine-elisa-kit-2762023115954.png)
![N/A IL-6 [HRP]](https://images.novusbio.com/fullsize/d6050b_human-il-6-quantikine-elisa-kit-276202312352.jpg)
![Western Blot: CD77 Synthase Antibody [NBP1-62583] - THP-1 cell lysate, concentration 0.2-1 ug/ml.](https://images.novusbio.com/fullsize/CD77-Synthase-Antibody-Western-Blot-NBP1-62583-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: MHC Class I Antibody (OX18) [NB120-6405] - Major histocompatibility complex (MHC) I and II as well as Transporter associated with antigen presentation II (TAPII) were analyzed, using immunocytochemistry on rat Schwann cells (SCs). Corresponding merges are shown in the bottom rows. Treatment of SCs with IL-17 was performed at concentrations of 0.5 and 50 ng/mL. Graphs to the right show densitometry quantification. SCs showed expression of MHCI > TAPII > MHCII, which increased after IL-17 treatment. MHCI was mainly detected in the cytoplasm and the expression increased in a dose-dependent manner after IL-17 treatment, significant for 0.5 ng/mL and 50 ng/mL (**P <=0.01). Image collected and cropped by CiteAb from the following publication (https://jneuroinflammation.biomedcentral.com/articles/10.1186/1742-2094-11-63), licensed under a CC-BY license.](https://images.novusbio.com/fullsize/MHC-Class-I-Antibody-OX18-Immunocytochemistry-Immunofluorescence-NB120-6405-img0009.jpg)
![Immunohistochemistry-Paraffin: MHC Class I Antibody (OX18) [NB120-6405] - Analysis of FFPE rat brain cerebellum using MHC Class I (OK18) antibody at 1:200 on a Bond Rx autostainer (Leica Biosystems). The assay involved 20 minutes of heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0) and endogenous peroxidase quenching with peroxide block. The sections were incubated with primary antibody for 30 minutes and Bond Polymer Refine Detection (Leica Biosystems) with DAB was used for signal development followed by counterstaining with hematoxylin. Whole slide scanning and capturing of representative images was performed using Aperio AT2 (Leica Biosystems). Endothelial staining was observed. Staining was performed by Histowiz.](https://images.novusbio.com/fullsize/MHC-Class-I-Antibody-OX18-Immunohistochemistry-Paraffin-NB120-6405-img0008.jpg)
![Western Blot: Aminomethyltransferase Antibody [NBP1-89783] - Analysis in human cell line HepG2.](https://images.novusbio.com/fullsize/Aminomethyltransferase-Antibody-Western-Blot-NBP1-89783-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: Aminomethyltransferase Antibody [NBP1-89783] - Staining of human cell line HeLa shows localization to nucleoplasm & mitochondria. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/Aminomethyltransferase-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-89783-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: Dystonin Antibody [NBP1-89946] - Staining of human cell line A-431 shows localization to nucleus & cytosol. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/Dystonin-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-89946-img0004.jpg)
![Immunohistochemistry-Paraffin: Dystonin Antibody [NBP1-89946] - Staining of human tonsil shows low positivity in non-germinal center cells as expected.](https://images.novusbio.com/fullsize/Dystonin-Antibody-Immunohistochemistry-Paraffin-NBP1-89946-img0008.jpg)
![Western Blot: Hsp47 Antibody (M16.10A1) [NBP1-97491] - analysis of Hsp47 in NIH/3T3 cell lysate (20ug/lane) using anti-Hsp47 antibody. 5x10^4 NIH/3T3 cells were seeded in 6-well plate and transfected with 50nM of HSP47 siRNA the following day. Total protein was harvested 72h after transfection. Image from verified customer review.](https://images.novusbio.com/fullsize/Hsp47-Antibody-M16-10A1-Western-Blot-NBP1-97491-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: Hsp47 Antibody (M16.10A1) [NBP1-97491] - WNT and BMP signaling pathways play crucial roles in regeneration. a-d Real-time PCR for WNT and BMP signals, including Wnt7b Dual immunostaining for K15 and phospho-Smad1/5 (pSmad1/5) revealed the nuclear staining of pSmad1/5 in hair stem cells at day 7 when skin was stretched (arrow). Scale bar?=?50?um. h, i Immunostaining and confocal microscope. Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/s41467-019-09402-8) licensed under a CC-BY license.](https://images.novusbio.com/fullsize/Hsp47-Antibody-M16-10A1-Immunocytochemistry-Immunofluorescence-NBP1-97491-img0007.jpg)
![Western Blot: HLA DQ/DR/DP Antibody (HLA-Pan/2967R) - Azide and BSA Free [NBP2-79843] - Western Blot Analysis of Ramos cell lysate using HLA DQ/DR/DP Antibody (HLA-Pan/2967R).](https://images.novusbio.com/fullsize/HLA-DQ-DR-DP-Antibody-HLA-Pan-2967R-Azide-and-BSA-Free-Western-Blot-NBP2-79843-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: HLA DQ/DR/DP Antibody (HLA-Pan/2967R) - Azide and BSA Free [NBP2-79843] - Immunofluorescence staining of PFA-fixed Ramos cells. HLA DQ/DR/DP Recombinant Rabbit Monoclonal Antibody (HLA DQ/DR/DP/2967R) followed by goat anti-rabbit IgG-CF488 (green). Nuclei stained with RedDot.](https://images.novusbio.com/fullsize/HLA-DQ-DR-DP-Antibody-HLA-Pan-2967R-Azide-and-BSA-Free-Immunocytochemistry-Immunofluorescence-NBP2-79843-img0006.jpg)
![Western Blot: OCA2 Antibody [NBP2-93603] - Analysis of extracts of various cell lines, using OCA2 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.](https://images.novusbio.com/fullsize/OCA2-Antibody-Western-Blot-NBP2-93603-img0001.jpg)