Regulation Of Seed Germination Pathway Bioinformatics
Disease and disorder research has been conducted in relation to the Regulation Of Seed Germination Pathway and Infective Disorder, Erectile Dysfunction, Photophobia, Malacia, Dehydration. The study of the Regulation Of Seed Germination Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Regulation Of Seed Germination Pathway has been researched in relation to Seed Germination, Germination, Hypersensitivity, Cell Wall Disassembly, Seedling Development. The Regulation Of Seed Germination Pathway complements our catalog of research reagents including antibodies and ELISA kits against AGA, GLS2, TNFSF14, RGL2, ABI1.
Top Research Reagents
We have 1461 products for the study of the Regulation Of Seed Germination Pathway that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: USP39 Antibody (1S9R9) [NBP3-16119] - Western blot analysis of extracts of Mouse liver, using USP39 antibody (NBP3-16119) 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: 1s.](https://images.novusbio.com/fullsize/USP39-Antibody-1S9R9-Western-Blot-NBP3-16119-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: USP39 Antibody (1S9R9) [NBP3-16119] - Immunofluorescence analysis of U2OS cells using USP39 Rabbit mAb (NBP3-16119) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/USP39-Antibody-1S9R9-Immunocytochemistry-Immunofluorescence-NBP3-16119-img0007.jpg)
![Western Blot: EPB42 Antibody (2G12) [H00002038-M01] - Analysis of EPB42 expression in transfected 293T cell line by EPB42 monoclonal antibody (M01), clone 2G12.Lane 1: EPB42 transfected lysate(69.5 KDa).Lane 2: Non-transfected lysate.](https://images.novusbio.com/fullsize/EPB42-Antibody-2G12-Western-Blot-H00002038-M01-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: EPB42 Antibody (2G12) [H00002038-M01] - Analysis of monoclonal antibody to EPB42 on HeLa cell . Antibody concentration 10 ug/ml.](https://images.novusbio.com/fullsize/EPB42-Antibody-2G12-Immunocytochemistry-Immunofluorescence-H00002038-M01-img0003.jpg)
![Western Blot: PTPLA Overexpression Lysate (Adult Normal) [NBL1-14964] Left-Empty vector transfected control cell lysate (HEK293 cell lysate); Right -Over-expression Lysate for PTPLA.](https://images.novusbio.com/fullsize/PTPLA-Overexpression-Lysate-Adult-Normal-Western-Blot-NBL1-14964-img0002.jpg)
![Western Blot: eRF1 Antibody [NBP1-31113] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with eRF1 antibody diluted at 1:500.](https://images.novusbio.com/fullsize/eRF1-Antibody-Western-Blot-NBP1-31113-img0010.jpg)
![Immunocytochemistry/Immunofluorescence: eRF1 Antibody [NBP1-31113] - A431 cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: eRF1 protein stained by eRF1 antibody diluted at 1:500. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [114] diluted at 1:1000. Blue: Hoechst 33342 staining.](https://images.novusbio.com/fullsize/eRF1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-31113-img0008.jpg)
![Western Blot: SUCLG2 Antibody [NBP1-32521] - Wild-type (WT) and SUCLG2 knockout (KO) 293T cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with SUCLG2 antibody diluted at 1:500. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://images.novusbio.com/fullsize/SUCLG2-Antibody-Western-Blot-NBP1-32521-img0013.jpg)
![Immunocytochemistry/Immunofluorescence: SUCLG2 Antibody [NBP1-32521] - HeLa cells were fixed in ice-cold MeOH for 5 min. Green: SUCLG2 protein stained by SUCLG2 antibody diluted at 1:500. Blue: Hoechst 33342 staining. Scale bar = 10 um.](https://images.novusbio.com/fullsize/SUCLG2-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-32521-img0012.jpg)
![Immunocytochemistry/Immunofluorescence: SUCLG1 Antibody [NBP1-32728] - Sample: HeLa cells were fixed in 2% paraformaldehyde/culture medium at 37C for 30 min. Green: SUCLG1 protein stained by SUCLG1 antibody diluted at 1:500. Blue: Hoechst 33342 staining.](https://images.novusbio.com/fullsize/SUCLG1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-32728-img0003.jpg)
![Immunohistochemistry-Paraffin: SUCLG1 Antibody [NBP1-32728] - N87 xenograft, using SUCLG1antibody at 1:100 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](https://images.novusbio.com/fullsize/SUCLG1-Antibody-Immunohistochemistry-Paraffin-NBP1-32728-img0004.jpg)
![Western Blot: Pancreatic Amylase Alpha Antibody (6D4) [NBP1-47659] - Pancreatic Amylase Alpha Antibody (6D4) HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Pancreatic Amylase(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-Pancreatic Amylase.](https://images.novusbio.com/fullsize/Pancreatic-Amylase-Alpha-Antibody-6D4-Western-Blot-NBP1-47659-img0022.jpg)
![Immunohistochemistry-Paraffin: Pancreatic Amylase Alpha Antibody (6D4) [NBP1-47659] - Pancreatic Amylase Alpha Antibody (6D4) Staining of paraffin-embedded ovary using anti-Pancreatic Amylase mouse monoclonal antibody.](https://images.novusbio.com/fullsize/Pancreatic-Amylase-Alpha-Antibody-6D4-Immunohistochemistry-Paraffin-NBP1-47659-img0021.jpg)
![Western Blot: GLS2 Antibody [NBP1-76544] - Glutaminase protein expression in PC3 and PC3M cell lines before/after CB-839 treatment. PC3 & PC3M cells were treated (+) or not treated (-) with GLS1 inhibitor CB-839 (1 uM) and their expression of GLS1 & GLS2 proteins determined by Western blot. Antibodies specific for GAC & KCA were utilized on two replicate samples, while GLS2 expression was determined on three. PC3 cell lysates expressed GLS2 more than PC3M cell lysates regardless of CB-839 treatment. The difference in GLS2 expression was significant in the untreated cells (P?<?0.03) but because of high variability the difference was not significant in the drug-treated cells. Levels of GLS1 (GAC and KGA) were similar in all cell lysates. Image collected and cropped by CiteAb from the following publication (https://www.nature.com/articles/s41598-017-16327-z), licensed under a CC-BY license.](https://images.novusbio.com/fullsize/GLS2-Antibody-Western-Blot-NBP1-76544-img0009.jpg)
![Immunocytochemistry/Immunofluorescence: GLS2 Antibody [NBP1-76544] - of GLS2 in Human Kidney cells. Dilution 20 ug/mL.](https://images.novusbio.com/fullsize/GLS2-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-76544-img0007.jpg)
![Immunohistochemistry-Paraffin: Biliverdin Reductase B/BLVRB Antibody [NBP1-83435] - Staining of human colon, liver, small intestine and spleen using Anti-BLVRB antibody NBP1-83435 (A) shows similar protein distribution across tissues to independent antibody NBP1-83434 (B).](https://images.novusbio.com/fullsize/Biliverdin-Reductase-B-BLVRB-Antibody-Immunohistochemistry-Paraffin-NBP1-83435-img0013.jpg)
![Western Blot: Biliverdin Reductase B/BLVRB Antibody [NBP1-83435] - Analysis in human cell lines A-549 and U-251MG. Corresponding RNA-seq data are presented for the same cell lines. Loading control: Anti-GAPDH.](https://images.novusbio.com/fullsize/Biliverdin-Reductase-B-BLVRB-Antibody-Western-Blot-NBP1-83435-img0010.jpg)
![Immunohistochemistry-Paraffin: SORBS1 Antibody [NBP1-86641] - Staining of human cerebral cortex, colon, lymph node and testis using Anti-SORBS1 antibody NBP1-86641 (A) shows similar protein distribution across tissues to independent antibody NBP2-33383 (B).](https://images.novusbio.com/fullsize/SORBS1-Antibody-Immunohistochemistry-Paraffin-NBP1-86641-img0008.jpg)
![Western Blot: SORBS1 Antibody [NBP1-86641] - Analysis in Caco-2 cells transfected with control siRNA, target specific siRNA probe #1 and #2,. Remaining relative intensity is presented. Loading control: Anti-GAPDH.](https://images.novusbio.com/fullsize/SORBS1-Antibody-Western-Blot-NBP1-86641-img0013.jpg)
![Immunohistochemistry-Paraffin: AGA Antibody [NBP1-88866] - Staining in human epididymis and skeletal muscle tissues using anti-AGA antibody. Corresponding AGA RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/AGA-Antibody-Immunohistochemistry-Paraffin-NBP1-88866-img0006.jpg)
![Immunohistochemistry-Paraffin: AGA Antibody [NBP1-88866] - Staining of human epididymis shows high expression.](https://images.novusbio.com/fullsize/AGA-Antibody-Immunohistochemistry-Paraffin-NBP1-88866-img0004.jpg)
![Western Blot: ERF Antibody [NBP2-16366] - Whole cell extract (30 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with ERF antibody (GTX114971) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](https://images.novusbio.com/fullsize/ERF-Antibody-Western-Blot-NBP2-16366-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: ERF Antibody [NBP2-16366] - HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: ERF stained by ERF antibody diluted at 1:500. Red: phalloidin, a cytoskeleton marker, diluted at 1:100. Scale bar= 10um.](https://images.novusbio.com/fullsize/ERF-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-16366-img0004.jpg)
![Western Blot: Glutathione S Transferase kappa 1 Antibody [NBP2-16686] - Wild-type (WT) and Glutathione S Transferase kappa 1 knockout (KO) 293T cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with Glutathione S Transferase kappa 1 antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://images.novusbio.com/fullsize/Glutathione-S-Transferase-kappa-1-Antibody-Western-Blot-NBP2-16686-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: Glutathione S Transferase kappa 1 Antibody [NBP2-16686] - Immunofluorescence analysis of methanol-fixed A549, using antibody at 1:500 dilution.](https://images.novusbio.com/fullsize/Glutathione-S-Transferase-kappa-1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-16686-img0003.jpg)
![Western Blot: RGL2 Antibody (4D10) [H00005863-M02] - Impact of RGL2 depletion on RalB activation at autophagosomes upon starvation. Validation of RGL2 depletions. Representative western blots for RGL2 and GAPDH from cell lysates of HEK-HT cells prepared 72 hrs after transfection with the indicated siRNAs. Quantifications of RGL2 protein depletion, normalized for siControl condition (=100), are shown below the WB. Image collected and cropped by CiteAb from the following publication (https://www.nature.com/articles/s41598-019-45443-1), licensed under a CC-BY license.](https://images.novusbio.com/fullsize/RGL2-Antibody-4D10-Western-Blot-H00005863-M02-img0009.jpg)
![Immunocytochemistry/Immunofluorescence: RGL2 Antibody (4D10) [H00005863-M02] - Analysis of monoclonal antibody to RGL2 on HeLa cell. Antibody concentration 10 ug/ml.](https://images.novusbio.com/fullsize/RGL2-Antibody-4D10-Immunocytochemistry-Immunofluorescence-H00005863-M02-img0005.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)
