Disease and disorder research has been conducted in relation to the Rejection Of Self Pollen Pathway and Hermaphroditism. The study of the Rejection Of Self Pollen Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Rejection Of Self Pollen Pathway has been researched in relation to Gametophytic Self-incompatibility, Transport, Pollen Hydration, Recognition Of Pollen, Fertilization. The Rejection Of Self Pollen Pathway complements our catalog of research reagents including antibodies and ELISA kits against SLF, PROTEIN FUSED, PSMD3, RPS3, RPS6KB2.
Top Research Reagents
We have 742 products for the study of the Rejection Of Self Pollen Pathway that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: p70 S6 Kinase beta/S6K2 Antibody (5D8F5) [NBP3-16752] - Western blot analysis of extracts of Mouse brain, using p70 S6 Kinase beta/S6K2 Rabbit mAb (NBP3-16752) 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: 3s.](https://images.novusbio.com/fullsize/p70-S6-Kinase-beta-S6K2-Antibody-5D8F5-Western-Blot-NBP3-16752-img0006.jpg)
![Immunocytochemistry/ Immunofluorescence: p70 S6 Kinase beta/S6K2 Antibody (5D8F5) [NBP3-16752] - Confocal imaging of C2C12 cells using p70 S6 Kinase beta/S6K2 Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) . The cells were counterstained with alpha-Tubulin Mouse mAb followed by incubation with ABflo 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.](https://images.novusbio.com/fullsize/nbp3-16752_rabbit-p70-s6-kinase-beta-s6k2-mab-5d8f5-822025209833.jpg)
![Immunocytochemistry/Immunofluorescence: RPS3 Antibody [NBP1-33691] - Analysis of methanol-fixed HeLa, using RPS3 antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with an alpha Tubulin antibody (Red) at 1:2000.](https://images.novusbio.com/fullsize/RPS3-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-33691-img0003.jpg)
![Immunohistochemistry-Paraffin: RPS3 Antibody [NBP1-33691] - Mouse intestine diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](https://images.novusbio.com/fullsize/RPS3-Antibody-Immunohistochemistry-Paraffin-NBP1-33691-img0009.jpg)
![Western Blot: Calcium Channel Flower Homolog Antibody [NBP1-84307] - Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10<br/>Lane 2: Negative control (vector only transfected HEK293T lysate)<br/>Lane 3: Over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (~3.1 kDa) in mammalian HEK293T cells, LY413631)](https://images.novusbio.com/fullsize/Calcium-Channel-Flower-Homolog-Antibody-Western-Blot-NBP1-84307-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: Calcium Channel Flower Homolog Antibody [NBP1-84307] - Staining of human cell line U-2 OS shows positivity in nucleus but not nucleoli. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/Calcium-Channel-Flower-Homolog-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-84307-img0004.jpg)
![Western Blot: ZAP70 Antibody [NBP1-87000] - Lane 1: Marker [kDa] 230, 110, 82, 49, 32, 26, 18. Lane 2: Human cell line RT-4. Lane 3: Human cell line U-251MG sp. Lane 4: Human plasma (IgG/HSA depleted). Lane 5: Human liver tissue. Lane 6: Human tonsil tissue](https://images.novusbio.com/fullsize/ZAP70-Antibody-Western-Blot-NBP1-87000-img0004.jpg)
![Immunohistochemistry-Paraffin: ZAP70 Antibody [NBP1-87000] - Staining of human lymph node shows high expression.](https://images.novusbio.com/fullsize/ZAP70-Antibody-Immunohistochemistry-Paraffin-NBP1-87000-img0006.jpg)
![Immunohistochemistry-Paraffin: SI Sucrase-Isomaltase Antibody [NBP1-87581] - Analysis in human small intestine and stomach tissues. Corresponding SI RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/SI-Sucrase-Isomaltase-Antibody-Immunohistochemistry-Paraffin-NBP1-87581-img0001.jpg)
![Western Blot: SI Sucrase-Isomaltase Antibody [NBP1-87581] - Analysis in human small intestine tissue.](https://images.novusbio.com/fullsize/SI-Sucrase-Isomaltase-Antibody-Western-Blot-NBP1-87581-img0006.jpg)
![Western Blot: PMEL17/SILV Antibody (HMB45) [NBP2-44520] - Western Blot Analysis of COLO-38 cell lysate using PMEL17/SILV antibody (HMB45).](https://images.novusbio.com/fullsize/PMEL17-SILV-Antibody-HMB45-Western-Blot-NBP2-44520-img0008.jpg)
![Immunohistochemistry: PMEL17/SILV Antibody (HMB45) [NBP2-44520] - PMEL17 (red) was detected in human skin (melanoma) using PMEL17-PE antibody (1:200) in PBS for 1 hour. Nuclei were stained with DAPI (blue). Image from a verified customer review. Image using the PE format of this antibody.](https://images.novusbio.com/fullsize/PMEL17-SILV-Antibody-HMB45-Immunohistochemistry-NBP2-44520-img0007.jpg)
![Western Blot: Proteasome 19S S3 Antibody (OTI2A2) - Azide and BSA Free [NBP2-73636] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Proteasome 19S S3 (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-Prot](https://images.novusbio.com/fullsize/Proteasome-19S-S3-Antibody-OTI2A2-Azide-and-BSA-Free-Western-Blot-NBP2-73636-img0002.jpg)
![Flow Cytometry: Proteasome 19S S3 Antibody (OTI2A2) - Azide and BSA Free [NBP2-73636] - HEK293T cells transfected with either overexpression plasmid (Red) or empty vector control plasmid (Blue) were immunostaining by anti-Proteasome 19S S3 antibody, and then analyzed by flow cytometry.](https://images.novusbio.com/fullsize/Proteasome-19S-S3-Antibody-OTI2A2-Azide-and-BSA-Free-Flow-Cytometry-NBP2-73636-img0005.jpg)
