Research of Psychoses, Substance-induced has been linked to Psychotic Disorders, Substance-related Disorders, Schizophrenia, Hallucinations, Mental Disorders. The study of Psychoses, Substance-induced has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Psychoses, Substance-induced include Sensitization, Pathogenesis, Excretion, Cognition, Hypersensitivity. These pathways complement our catalog of research reagents for the study of Psychoses, Substance-induced including antibodies and ELISA kits against SGSM3, POMC, PRCP, IFNA1, PGPEP1.
Top Research Reagents
We have 1550 products for the study of Psychoses, Substance-induced that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: Dopamine D2R/DRD2 Antibody (HL1478) - Azide and BSA Free [NBP3-25443] - Various tissue extracts (30 ug) were separated by 10% SDS-PAGE, and the membranes were blotted with Dopamine Receptor D2 antibody [HL1478] (NBP3-25443) diluted at 1:1000 and competitor's antibody (Ab5084p) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://images.novusbio.com/fullsize/nbp3-25443_rabbit-dopamine-d2r-drd2-mab-hl1478-azide-and-bsa-free-2120249403851.jpg)
![Western Blot: Dopamine D2R/DRD2 Antibody (HL1478) - Azide and BSA Free [NBP3-25443] - Unboiled mouse tissue extract (30 ug) was separated by 10% SDS-PAGE, and the membranes were blotted with Dopamine Receptor D2 antibody [HL1478] (NBP3-25443) diluted at 1:500 and competitor's antibody (Ab5084p) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://images.novusbio.com/fullsize/nbp3-25443_rabbit-dopamine-d2r-drd2-mab-hl1478-azide-and-bsa-free-212024941490.jpg)
![Immunocytochemistry/Immunofluorescence: DIO2 Antibody [NBP1-00178] - Analysis of paraformaldehyde fixed HeLa cells, permeabilized with 0.15% Triton.Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing nuclear and cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).](https://images.novusbio.com/fullsize/DIO2-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-00178-img0006.jpg)
![Immunohistochemistry-Frozen: DIO2 Antibody [NBP1-00178] - IHC analysis of DIO2 in cryo-sectioned Mouse Hippocampus using NBP1-00178 at 2ug/ml. Microwaved antigen retrieval with citrate buffer pH 4.5, HRP-staining.](https://images.novusbio.com/fullsize/DIO2-Antibody-Immunohistochemistry-Frozen-NBP1-00178-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: Cannabinoid R1/CB1/CNR1 Antibody [NLS32] - Analysis of anti-CNR1 / CB1 antibody with HEK293 human embryonic kidney cells.](https://images.novusbio.com/fullsize/Cannabinoid-R1-CB1-CNR1-Antibody-Immunocytochemistry-Immunofluorescence-NLS32-img0007.jpg)
![Immunohistochemistry-Paraffin: Cannabinoid R1/CB1/CNR1 Antibody [NLS32] - Brain, substantia nigra](https://images.novusbio.com/fullsize/Cannabinoid-R1-CB1-CNR1-Antibody-Immunohistochemistry-Paraffin-NLS32-img0013.jpg)
![Western Blot: Dopamine beta-Hydroxylase Antibody [NBP1-31386] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membranes were blotted with Dopamine beta hydroxylase antibody and a competitor's antibody. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://images.novusbio.com/fullsize/Dopamine-beta-Hydroxylase-Antibody-Western-Blot-NBP1-31386-img0017.jpg)
![Immunohistochemistry-Paraffin: Dopamine beta-Hydroxylase Antibody [NBP1-31386] - RT2 xenograft. Dopamine beta hydroxylase antibody dilution: 1:500. Antigen Retrieval: Trilogy&#8482; (EDTA based, pH 8.0) buffer, 15min.](https://images.novusbio.com/fullsize/Dopamine-beta-Hydroxylase-Antibody-Immunohistochemistry-Paraffin-NBP1-31386-img0013.jpg)
![Immunocytochemistry/Immunofluorescence: GlyT1/SLC6A9 Antibody [NBP1-81820] - Staining of human cell line U-251 MG shows localization to nucleoplasm & the Golgi apparatus. Antibody staining is shown in green](https://images.novusbio.com/fullsize/GlyT1-SLC6A9-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-81820-img0008.jpg)
![Immunohistochemistry-Paraffin: GlyT1/SLC6A9 Antibody [NBP1-81820] - Staining of human cervix, uterine shows no positivity in squamous epithelial cells as expected.](https://images.novusbio.com/fullsize/GlyT1-SLC6A9-Antibody-Immunohistochemistry-Paraffin-NBP1-81820-img0012.jpg)
![Immunocytochemistry/Immunofluorescence: WASP Antibody [NB300-996] - Immunofluorescence analysis of paraformaldehyde fixed U2OS cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing nuclear and cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](https://images.novusbio.com/fullsize/WASP-Antibody-Immunocytochemistry-Immunofluorescence-NB300-996-img0007.jpg)
![Immunohistochemistry-Paraffin: WASP Antibody [NB300-996] - Staining of paraffin embedded Human Spleen. Antibody at 5 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.](https://images.novusbio.com/fullsize/WASP-Antibody-Immunohistochemistry-Paraffin-NB300-996-img0004.jpg)
![Western Blot: COMT Antibody [NB100-1780] - Staining of MCF7 (A) with antibody at 0.5 ug/mL, U251 cell lysate 1 (B) and U251 cell lysate 2 (C) (35 ug protein in RIPA buffer) with antibody at 1 ug/mL. Detected by chemiluminescence.](https://images.novusbio.com/fullsize/COMT-Antibody-Western-Blot-NB100-1780-img0002.jpg)
![Flow Cytometry: COMT Antibody [NB100-1780] - Flow cytometric analysis of paraformaldehyde fixed A431 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (1 ug/mL). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody.](https://images.novusbio.com/fullsize/COMT-Antibody-Flow-Cytometry-NB100-1780-img0003.jpg)
![Western Blot: SGSM3 Antibody [NBP2-13304] - Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10. Lane 2: Human cell line RT-4](https://images.novusbio.com/fullsize/SGSM3-Antibody-Western-Blot-NBP2-13304-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: SGSM3 Antibody [NBP2-13304] - Immunofluorescent staining of human cell line MCF7 shows localization to the Golgi apparatus.](https://images.novusbio.com/fullsize/SGSM3-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-13304-img0005.jpg)
![Western Blot: SLC6A3/DAT1 Antibody (mAb16) [NBP2-22164] - Western blot analysis of DAT protein. Band shown at approx. 75 kDa. Image submitted by verified customer review.](https://images.novusbio.com/fullsize/SLC6A3-DAT1-Antibody-mAb16-Western-Blot-NBP2-22164-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: DAT1 Antibody (mAb16) [NBP2-22164] - The DAT1 antibody was tested in PC12 cells at a 1:250 dilution against DyLight 488 (Green). Actin and nuclei were counterstained with Phalloidin-AlexaFluor 568 (Red) and DAPI (Blue), respectively.](https://images.novusbio.com/fullsize/DAT1-Antibody-mAb16-Immunocytochemistry-Immunofluorescence-NBP2-22164-img0004.jpg)
![Immunohistochemistry: POMC Antibody [NB100-1533] - Representative confocal images of POMC in POMC-transfected WT and Sel1L-/- N2a cells. White arrows point to POMC-containing secretory granules, while yellow arrows point to perinuclear POMC. KDEL marks the ER. Representative data from at least 2 independent experiments are shown. Image collected and cropped by CiteAb from the following publication (jci.org/articles/view/96420), licensed under a CC-BY license.](https://images.novusbio.com/fullsize/POMC-Antibody-Immunohistochemistry-NB100-1533-img0008.jpg)
![Flow Cytometry: POMC Antibody [NB100-1533] - Flow cytometric analysis of paraformaldehyde fixed A431 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (1 ug/mL). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody.](https://images.novusbio.com/fullsize/POMC-Antibody-Flow-Cytometry-NB100-1533-img0006.jpg)
![Immunohistochemistry-Paraffin: LAMC2 Antibody (CL2980) [NBP2-42388] - Staining in human fallopian tube and liver tissues. Corresponding LAMC2 RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/LAMC2-Antibody-CL2980-Immunohistochemistry-Paraffin-NBP2-42388-img0023.jpg)
![Western Blot: LAMC2 Antibody (CL2980) [NBP2-42388] - Analysis in A-431 cells transfected with control siRNA, target specific siRNA probe #1 and #2, using Anti-LAMC2 antibody. Remaining relative intensity is presented. Loading control: Anti-GAPDH.](https://images.novusbio.com/fullsize/LAMC2-Antibody-CL2980-Western-Blot-NBP2-42388-img0017.jpg)
![Western Blot: IFN-alpha 1 Antibody [NBP2-75930] - analysis of IFNA1 on mouse liver tissue lysate using anti-IFNA1 antibody at 1/100 dilution.](https://images.novusbio.com/fullsize/IFN-alpha-1-Antibody-Western-Blot-NBP2-75930-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: IFN-alpha 1 Antibody [NBP2-75930] - staining IFNA1 in SH-SY5Y 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/IFN-alpha-1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-75930-img0004.jpg)
![Western Blot: SLC6A4/5-HTTLPR/Serotonin transporter Antibody [NBP3-05546] - Different tissue and cell lysates using NBP3-05546 at a dilution of 1:1,000 in green. Left: [1] protein standard, [2] rat brain caudate/putmen region, [3] rat brain striatum region and [4] mouse brain. The prominent band at ~68kDa corresponds to SLC6A4 protein, and lower bands are likely are proteolytic products of SLC6A4. [5] protein standard, [6] non-transfected HEK293 cells and [7] HEK293 cells transfected with an expression construct containing a Myc-DDK tagged full length human SLC6A4 cDNA. The bands between 50-75kDa mark in the transfected cells demonstrate overexpression of SLC6A4, and the band at about 150kDa presumably corresponds to an aggregated form of SLC6A4. The blot was probed with mouse mAb to GAPDH at a dilution of 1:5,000, in red, which reveals the single band at ~37kDa in both transfected and non-transfected cells. Note that HEK293 cells express endogenously (7).](https://images.novusbio.com/fullsize/SLC6A4-5-HTTLPR-Serotonin-transporter-Antibody-Western-Blot-NBP3-05546-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: SLC6A4/5-HTTLPR/Serotonin transporter Antibody [NBP3-05546] - Immunofluorescent analysis of a rat brain section stained with SLC6A4/5-HTTLPR/Serotonin transporter Antibody in green and counterstained with chicken polyclonal antibody to tyrosine hydroxylase in red. The axons of serotoninergic neurons course throughout the section but are clearly distinct from the chatacholinergic processes and cell bodies revealed with the TH antibody. The blue stain reveals DNA in cell nuclei.](https://images.novusbio.com/fullsize/SLC6A4-5-HTTLPR-Serotonin-transporter-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05546-img0001.jpg)
