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Regulation Of Protein Processing Pathway Bioinformatics

Disease and disorder research has been conducted in relation to the Regulation Of Protein Processing Pathway and Abnormal Degeneration, Adenocarcinoma, Malignant Neoplasm Of Prostate, Malignant Neoplasms, Prostatic Neoplasms. The study of the Regulation Of Protein Processing Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Regulation Of Protein Processing Pathway has been researched in relation to Protein Processing, Proteolysis, Transport, Protein Glycosylation, Glycosylation. The Regulation Of Protein Processing Pathway complements our catalog of research reagents including antibodies and ELISA kits against NOS2, CREB3L4, ATF6, BAG3, KDELR3.

Regulation Of Protein Processing Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Regulation Of Protein Processing below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 310 products for the study of the Regulation Of Protein Processing Pathway that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NB300-605
Western Blot: iNOS Antibody [NB300-605] - Analysis of iNOS was performed by loading 20 ug of RAW264 whole cell lysate untreated (left lane) or stimulated with LPS at 1 ug/mL for 16 hours (right lane) and 10 uL of PageRuler Plus Prestained Protein Ladder onto a 4-20% Tris-Glycine polyacrylamide gel. Proteins were transferred to a nitrocellulose membrane and blocked with 5% Milk in TBST for at least 1 hour. The membrane was probed with an iNOS Rabbit polyclonal antibody at a dilution of 1:1000 overnight at 4C on a rocking platform, washed in TBST, and probed with a Goat anti-Rabbit IgG (H+L) Secondary Antibody, HRP conjugate at a dilution of 1:1000 for 1 hour. Chemiluminescent detection was performed using SuperSignal West Pico.Immunohistochemistry-Paraffin: iNOS Antibody [NB300-605] - Immunohistochemistry was performed on normal deparaffinized human Lung tissue.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, Flow, IB

     3 Reviews

65 Publications
H00148327-M01
Western Blot: AIBZIP Antibody (3E3) [H00148327-M01] - Analysis of CREB3L4 over-expressed 293 cell line, cotransfected with CREB3L4 Validated Chimera RNAi ( Cat # H00148327-R01V ) (Lane 2) or non-transfected control (Lane 1). Blot probed with CREB3L4 monoclonal antibody (M01), clone 3E3 (Cat # H00148327-M01 ). GAPDH ( 36.1 kDa ) used as specificity and loading control.Immunocytochemistry/Immunofluorescence: AIBZIP Antibody (3E3) [H00148327-M01] - Analysis of monoclonal antibody to CREB3L4 on HeLa cell. Antibody concentration 10 ug/ml.

Mouse Monoclonal
Species Human
Applications WB, ELISA, ICC/IF

NBP1-40256
Western Blot: ATF6 Antibody (70B1413.1) [NBP1-40256] - Hypoxia leads to EMT and ER-stress in CRC cells. B. C. Confluent growing SW480 (B) and HCT116 (C) cells were cultured under conditions of normoxia or hypoxia-like conditions (serum free; 100 uM CoCl2, 1-9 h. B-actin (B-act) as loading control. HIF1a was detectable after 3 h of CoCl2 incubation, the amount of the 50 kD-ATF6 fragment, was already enhanced after 1 h of addition of CoCl2. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0087386) licensed under a CC-BY licence.Western Blot: ATF6 Antibody (70B1413.1) [NBP1-40256] - Analysis of  ATF6 in mouse liver tissue using 3 ug/ml of ATF6 antibody and 0.25 ug/ml of GAPDH antibody.  Lane A contains 20 ugs of whole mouse liver lysate, lane B contains 20 ugs of total ER fraction, and lane C contains 20 ugs of rough ER fraction. The ATF6 band may represent under glycosylated or cleaved/active ATF6.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, ChIP, Flow

     2 Reviews

205 Publications
NBP2-27398
Western Blot: BAG3 Antibody [NBP2-27398] - Analysis of BAG3 using NBP2-27398 at 1:2000. Tissue lysates, normalized for total protein (20 ug/lane), were from a 4 week old male mouse. BAG-3 expression was detected at highest levels in skeletal (quadriceps and diaphragm) and smooth (heart) muscle specimens.Immunocytochemistry/Immunofluorescence: BAG3 Antibody [NBP2-27398] - Antibody was tested in A431 cells with DyLight 488 (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and DyLight 550 (red).

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, Simple Western, ICC/IF

7 Publications
H00011015-P01
12.5% SDS-PAGE Stained with Coomassie Blue.


Species Human

NBP1-76917
Western Blot: Nanos2 Antibody [NBP1-76917] - Rat brain tissue lysate with Nanos2 antibody at (A) 1 and (B) 2 ug/mL.Immunocytochemistry/Immunofluorescence: Nanos2 Antibody [NBP1-76917] - Immunofluorescence of Nanos2 in Human Testis cells with Nanos2 antibody at 20 ug/mL.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ELISA, ICC/IF

NBP1-57718
Western Blot: DNAJC12 Antibody [NBP1-57718] - THP-1 cell lysate, concentration 0.2-1 ug/ml.

Rabbit Polyclonal
Species Human
Applications WB

1 Publication
NBP1-47790
Western Blot: Goosecoid Antibody (1D7) [NBP1-47790] - Analysis of extracts (35ug) from 9 different cell lines by using anti-GSC monoclonal antibody.Immunohistochemistry-Paraffin: Goosecoid Antibody (1D7) [NBP1-47790] -  Staining of paraffin-embedded Human prostate tissue using anti-GSC mouse monoclonal antibody.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, Flow, IHC

NBP2-47415
Western Blot: ISYNA1 Antibody [NBP2-47415] - Lane 1: Marker [kDa] 250, 130, 100, 70, 55, 35, 25, 15, 10<br/>Lane 2: Human cell line HEK 293Immunocytochemistry/Immunofluorescence: ISYNA1 Antibody [NBP2-47415] - Immunofluorescent staining of human cell line HEK 293 shows localization to nucleus & cytosol.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, IHC


Related Genes

The Regulation Of Protein Processing Pathway has been researched against:

Related Pathways

The Regulation Of Protein Processing Pathway has been linked to:

Related Diseases

The Regulation Of Protein Processing Pathway has been studied in relation to diseases such as:

Related PTMs

The Regulation Of Protein Processing Pathway has been studied in relation to posttranslational modifications (PTMs) including: