Disease and disorder research has been conducted in relation to the Fruit Dehiscence Pathway and Prolymphocytic Leukemia, Growth Arrest. The study of the Fruit Dehiscence Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Fruit Dehiscence Pathway has been researched in relation to Dehiscence, Abscission, Transport, Fruit Development, Fruit Abscission. The Fruit Dehiscence Pathway complements our catalog of research reagents including antibodies and ELISA kits against AG, PG, ACACA, GUSB, MAPT.
Top Research Reagents
We have 1236 products for the study of the Fruit Dehiscence Pathway that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: c-Myc Antibody (9E10) [NB600-302] - CtIP is phosphorylated by CDKs at multiple sites. Myc-BRCA1 and/or HA-CtIP WT or indicated mutants were expressed in 293T cells and co-immunoprecipitation was performed. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pgen.1003277) licensed under a CC-BY license.](https://images.novusbio.com/fullsize/c-Myc-Antibody-9E10-Western-Blot-NB600-302-img0022.jpg)
![Immunohistochemistry-Paraffin: c-Myc Antibody (9E10) [NB600-302] - c-Myc was detected in immersion fixed paraffin-embedded sections of human breast cancer using anti-human mouse monoclonal antibody (Catalog # NB600-302, clone 9E10) at 1:50 dilution overnight at 4 C. Tissue was stained using the VisuCyte anti-mouse HRP polymer detection reagent (Catalog # VC001) with DAB chromogen (brown) and counterstained with hematoxylin (blue). <br/>Images may not be copied, printed or otherwise disseminated without express written permission of Novus Biologicals a bio-techne brand.](https://images.novusbio.com/fullsize/c-Myc-Antibody-9E10-Immunohistochemistry-Paraffin-NB600-302-img0009.jpg)
![Immunohistochemistry-Paraffin: SHP/NR0B2/Nuclear Receptor SHP Antibody [NLS5411] - Breast, carcinoma](https://images.novusbio.com/fullsize/SHP-NR0B2-Nuclear-Receptor-SHP-Antibody-Immunohistochemistry-Paraffin-NLS5411-img0007.jpg)
![Immunohistochemistry-Paraffin: SHP/NR0B2/Nuclear Receptor SHP Antibody [NLS5411] - Analysis of anti-NR0B2 antibody with human liver, hepatocytes.](https://images.novusbio.com/fullsize/SHP-NR0B2-Nuclear-Receptor-SHP-Antibody-Immunohistochemistry-Paraffin-NLS5411-img0004.jpg)
![Western Blot: ABCB6 Antibody [NBP3-41339] - Sample: Recombinant protein.](https://images.novusbio.com/fullsize/nbp3-41339_rabbit-abcb6-pab-612202421283894.jpg)
![Immunohistochemistry-Paraffin: ABCB6 Antibody [NBP3-41339] - Vector Red staining on IHC-P; Samples: Human Testis Tissue; Primary Ab: 10ug/ml NBP3-41339; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody](https://images.novusbio.com/fullsize/nbp3-41339_rabbit-abcb6-pab-612202421395378.jpg)
![Western Blot: ALLC Antibody [H00055821-D01P] - Analysis of ALLC expression in mouse brain.](https://images.novusbio.com/fullsize/ALLC-Antibody-Western-Blot-H00055821-D01P-img0003.jpg)
![Western Blot: ALLC Antibody [H00055821-D01P] - Analysis of ALLC expression in MCF-7.](https://images.novusbio.com/fullsize/ALLC-Antibody-Western-Blot-H00055821-D01P-img0001.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)
![Immunohistochemistry-Paraffin: beta-Glucuronidase/GUSB Antibody [NBP1-87511] - Analysis in human liver and skeletal muscle tissues using NBP1-87511 antibody. Corresponding GUSB RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/beta-Glucuronidase-GUSB-Antibody-Immunohistochemistry-Paraffin-NBP1-87511-img0009.jpg)
![Western Blot: beta-Glucuronidase/GUSB Antibody [NBP1-87511] - Analysis in control (vector only transfected HEK293T lysate) and GUSB over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).](https://images.novusbio.com/fullsize/beta-Glucuronidase-GUSB-Antibody-Western-Blot-NBP1-87511-img0007.jpg)
![Western Blot: Tau Antibody (2E9) [NBP2-25162] - Analysis of different tissue lysates using mouse mAb to MAP-tau, NBP2-25162, dilution 1:2,000 in green: [1] protein standard (red), [2] rat brain, [3] rat spinal cord, [4] mouse brain, [5] mouse spinal cord. Tau protein is expressed as up to 9 different isoforms of different molecular weight, and so appears as multiple closely spaced bands in the range from 48 kDa to 67 kDa in the CNS and including larger big tau forms in the PNS, visible in lane 5.](https://images.novusbio.com/fullsize/Tau-Antibody-2E9-Western-Blot-NBP2-25162-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: Tau Antibody (2E9) [NBP2-25162] - Analysis of cortical neuron-glial culture from E20 rat stained with mouse mAb to MAP-tau, NBP2-25162, dilution 1:1,000 in green, and costained with chicken pAb to MAP2, dilution 1:5,000 in red. The blue is DAPI staining of nuclear DNA. NBP2-25162 antibody stains perikarya, dendrites and axons of neurons, while MAP2 antibody labels only dendrites and perikarya. As a result, perikarya and dendrites appear orange-yellow, since they contain both proteins.](https://images.novusbio.com/fullsize/Tau-Antibody-2E9-Immunocytochemistry-Immunofluorescence-NBP2-25162-img0005.jpg)
![Western Blot: SHP-1 Antibody (SR41-02) [NBP2-67321] - Analysis of SHP1 on different 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 at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Raji cell lysate Lane 2: Jurkat cell lysate](https://images.novusbio.com/fullsize/SHP-1-Antibody-SR41-02-Western-Blot-NBP2-67321-img0010.jpg)
![Immunocytochemistry/Immunofluorescence: SHP-1 Antibody (SR41-02) [NBP2-67321] - Staining SHP1 in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](https://images.novusbio.com/fullsize/SHP-1-Antibody-SR41-02-Immunocytochemistry-Immunofluorescence-NBP2-67321-img0003.jpg)
