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Food Poisoning Due To Clostridium Perfringens: Disease Bioinformatics

Research of Food Poisoning Due To Clostridium Perfringens has been linked to Food Poisoning, Poisoning, Foodborne Disease, Clostridium Infections, Diarrhea. The study of Food Poisoning Due To Clostridium Perfringens has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Food Poisoning Due To Clostridium Perfringens include Germination, Sporulation, Spore Germination. These pathways complement our catalog of research reagents for the study of Food Poisoning Due To Clostridium Perfringens including antibodies and ELISA kits against TXN, ASPRV1, LYZ, CPE, SPM.

Food Poisoning Due To Clostridium Perfringens 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 Food Poisoning Due To Clostridium Perfringens below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 433 products for the study of Food Poisoning Due To Clostridium Perfringens that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP2-52983
Immunocytochemistry/Immunofluorescence: Thioredoxin Antibody [NBP2-52983] - HeLa cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X TBS + 0.5% Triton-X100. The cells were incubated with anti-Thioredoxin at a 1:100 dilution overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:500 dilution. Alpha tubulin (DM1A) [NB100-690] was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse Dylight 550 (Red) at a 1:500 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.Immunocytochemistry/Immunofluorescence: Thioredoxin Antibody [NBP2-52983] - NIH-3T3 cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X PBS + 0.05% Triton-X100. The cells were incubated with anti-Thioredoxin at 5 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:500 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, Flow, ICC/IF

NBP2-33981
Immunohistochemistry-Paraffin: ASPRV1 Antibody [NBP2-33981] - Staining of human colon.Immunohistochemistry-Paraffin: ASPRV1 Antibody [NBP2-33981] - Staining of human skeletal muscle shows low expression as expected.

Rabbit Polyclonal
Species Human, Canine
Applications ICC/IF, IHC, IHC-P

1 Publication
NBP2-61118
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.Immunocytochemistry/Immunofluorescence: Lysozyme Antibody [NBP2-61118] - HeLa cells were fixed and permeabilized for 10 minutes using -20C MeOH. The cells were incubated with anti-Lysozyme at 2 ug/ml overnight at 4C and detected with an anti-rabbit DyLight 488 (Green) at a 1:500 dilution. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse DyLight 550 (Red) at a 1:500 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, Simple Western, Flow

1 Publication
AF3587
<P align=left>A172 human glioblastoma cell line was stained with Goat Anti-Human Carboxypeptidase E/CPE Antigen Affinity‑purified Polyclonal Antibody (Catalog # AF3587, filled histogram) or control antibody (Catalog # <A class=NoLineLink href=<P align=left>Carboxypeptidase E/CPE was detected in immersion fixed HepG2 human hepatocellular carcinoma cell line using Goat Anti-Human Carboxypeptidase E/CPE Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3587) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red, upper panel; Catalog # <A class=NoLineLink href=

Goat Polyclonal
Species Human
Applications WB, IHC, IP

NBP1-87974
Western Blot: CSP Antibody [NBP1-87974] - Lane 1: Marker  [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11.  Lane 2: Human cell line RT-4.  Lane 3: Human cell line U-251MG spImmunohistochemistry-Paraffin: CSP Antibody [NBP1-87974] - Staining of human skeletal muscle shows no positivity in myocytes as expected.

Rabbit Polyclonal
Species Human
Applications WB, IHC, IHC-P

NB100-684
Immunocytochemistry/Immunofluorescence: Granzyme B Antibody [NB100-684] - Staining of Granzyme B in red on FFPE human Tonsil. Secondary antibody is donkey anti-rabbit A647. Nuclei counter-stained with DAPI. Staining pattern is cytoplasmic with obvious polarization (see arrowheads) in some cases. This image was submitted via customer Review.Immunohistochemistry-Paraffin: Granzyme B Antibody [NB100-684] - FFPE human tonsil stained with Granzyme B antibody.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications ICC/IF, IHC, IHC-Fr

     1 Review

6 Publications

Related Genes

Food Poisoning Due To Clostridium Perfringens has been researched against:

Related Pathways

Food Poisoning Due To Clostridium Perfringens has been linked to:

Alternate Names

Food Poisoning Due To Clostridium Perfringens is also known as Clostridium Perfringens Food Poisoning, Clostridium Perfringens Gastroenteritis, Perfringens Gastroenteritis.