Disease and disorder research has been conducted in relation to the Protein Digestion Pathway and Malignant Neoplasms, Shwachman Syndrome, Neoplasms, Celiac Disease, Infective Disorder. The study of the Protein Digestion Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Protein Digestion Pathway has been researched in relation to Proteolysis, Secretion, Transport, Excretion, Localization. The Protein Digestion Pathway complements our catalog of research reagents including antibodies and ELISA kits against MILK PROTEIN, CE, OVALBUMIN, ALB, ANPEP.
Top Research Reagents
We have 2045 products for the study of the Protein Digestion Pathway that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![ELISA: Pepsinogen I Antibody (HL2137) - Azide and BSA Free [NBP3-25594] - Indirect ELISA analysis was performed by coating the plate with recombinant NS0 cells expressed, full-length human pepsinogen A protein (97.56-1.52 nM). Coated protein was probed with Pepsinogen I antibody [HL2137] (NBP3-25594) (1 ug/mL). Goat anti-rabbit IgG antibody (HRP) (1:10000) was used to detect the bound primary antibody.](https://images.novusbio.com/fullsize/nbp3-25594_rabbit-pepsinogen-i-mab-hl2137-azide-and-bsa-free-212024941410.jpg)
![Western Blot: Pepsinogen I Antibody (HL2137) - Azide and BSA Free [NBP3-25594] - Various tissue extracts (10 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Pepsinogen I antibody [HL2137] (NBP3-25594) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://images.novusbio.com/fullsize/nbp3-25594_rabbit-pepsinogen-i-mab-hl2137-azide-and-bsa-free-2120249374963.jpg)
![Immunohistochemistry-Paraffin: Glutaminyl-peptide Cyclotransferase/QPCT Antibody [NBP1-81838] - Staining in human adrenal gland and liver tissues using anti-QPCT antibody. Corresponding QPCT RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/Glutaminyl-peptide-Cyclotransferase-QPCT-Antibody-Immunohistochemistry-Paraffin-NBP1-81838-img0010.jpg)
![Western Blot: Glutaminyl-peptide Cyclotransferase/QPCT Antibody [NBP1-81838] - Analysis in human cell line SK-MEL-30.](https://images.novusbio.com/fullsize/Glutaminyl-peptide-Cyclotransferase-QPCT-Antibody-Western-Blot-NBP1-81838-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: PEPT1/SLC15A1 Antibody [NBP1-92005] - Staining of human cell line CACO-2 shows localization to nucleoplasm. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/PEPT1-SLC15A1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-92005-img0004.jpg)
![Immunohistochemistry-Paraffin: PEPT1/SLC15A1 Antibody [NBP1-92005] - Staining of human small intestine shows strong membranous and moderate cytoplasmic positivity in glandular cells.](https://images.novusbio.com/fullsize/PEPT1-SLC15A1-Antibody-Immunohistochemistry-Paraffin-NBP1-92005-img0005.jpg)
![N/A Trappin-2/Elafin/Skalp [Biotin]](https://images.novusbio.com/fullsize2/DATA_Trappin2_DY1747_ELISA_1708.jpg)
![Western Blot: Pepsinogen A Antibody (961902) [MAB9350] - Analysis of human stomach tissue lysate with 2 ug/ml of hPGA-4 Monoclonal Antibody followed by HAF005. A specific band was detected for hPGA-4 at approximately45 kDA (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.](https://images.novusbio.com/fullsize/Pepsinogen-A-Antibody-961902-Western-Blot-MAB9350-img0001.jpg)
![Immunohistochemistry: Pepsinogen A Antibody (961902) [MAB9350] - Pepsinogen A was detected in immersion fixed paraffin-embedded sections of human stomach using Pepsinogen A Monoclonal Antibody at 1.7 ug/ml. Tissue was stained using Rat IgG VisUCyte HRP Polymer Antibody (brown) and counterstained with hematoxylin (blue). Specific staining was localized to the cytoplasm in epithelial cells.](https://images.novusbio.com/fullsize/Pepsinogen-A-Antibody-961902-Immunohistochemistry-MAB9350-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: Lysozyme Antibody [NBP2-61118] - NIH3T3 cells were fixed and permeabilized for 10 minutes using -20C MeOH. The cells were incubated with anti-Lysozyme NBP2-61118 at 2 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](https://images.novusbio.com/fullsize/Lysozyme-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-61118-img0006.jpg)
![Western Blot: Lysozyme Antibody [NBP2-61118] - Total protein from human cell lines THP-1 and HepG2, human stomach and kidney as well as mouse kidney was separated on a 4-20% gel by SDS-PAGE, transferred to 0.2 um PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2.0 ug/ml anti-Lysozyme in 5% non-fat milk in TBST and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.](https://images.novusbio.com/fullsize/Lysozyme-Antibody-Western-Blot-NBP2-61118-img0003.jpg)
![Western Blot: Cytochrome c Antibody (7H8.2C12) [NB100-56503] - Metformin activates apoptotic cell death; Right panel: MCF-7 cells were kept in the presence or absence of metformin for 20 days and then processed to obtain mitochondrial or whole cellular extracts. BAX and CYCS expression levels were determined by Western blot as indicated under Material and Methods. Densitometric analysis of the gels was performed as indicated under Material and Methods. PHB and CDK4 were used as purity and loading controls. Image collected and cropped by CiteAb from the following publication (https://www.mdpi.com/2073-4409/8/1/49), licensed under a CC-BY license.](https://images.novusbio.com/fullsize/Cytochrome-c-Antibody-7H8-2C12-Western-Blot-NB100-56503-img0015.jpg)
![Immunocytochemistry/Immunofluorescence: Cytochrome c Antibody (7H8.2C12) [NB100-56503] - p73 was detected in immersion fixed Hela human cell line using NB100-56503 at 25 ug/ml for 3 hours at room temperature. Cells were stained using the NorthernLights(TM) 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # NL007) and counterstained with DAPI (blue). Staining was observed in the cytoplasm and mitochondria.](https://images.novusbio.com/fullsize/Cytochrome-c-Antibody-7H8-2C12-Immunocytochemistry-Immunofluorescence-NB100-56503-img0010.jpg)
![Western Blot: TEF1 Antibody [NBP2-94035] - Analysis of extracts of various cell lines, using TEAD1 antibody 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/TEF1-Antibody-Western-Blot-NBP2-94035-img0012.jpg)
![Immunocytochemistry/Immunofluorescence: TEF1 Antibody [NBP2-94035] - Analysis of MCF7 cells using TEF1 .](https://images.novusbio.com/fullsize/TEF1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-94035-img0002.jpg)
