Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed)
Novus Biologicals | Catalog # NBP1-75617
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Description
Product is stable for up to 4 weeks at 2-8C after rehydration. For extended storage after rehydration, add an equal volume of glycerol and store at -20C.
Scientific Data Images
Immunocytochemistry/ Immunofluorescence: Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed) [NBP1-75617] -
Immunocytochemistry/ Immunofluorescence: Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed) [NBP1-75617] - Effect of varied WAT masses from obese mice on vimentin & CD24 protein expression in MDA-MB-231 cells. (a) Representative images of MDA-MB-231 cells cultured with or without 200 mg or 800 mg of obese subcutaneous or visceral WAT-CM & co-stained with anti-vimentin, anti-CD24, & DAPI; scale bar = 100 µm. (b) & (c) are the relative expression of the respective markers, mean ± SEM (n = 6 biological replicates). The average protein expression from five images per replicate were normalized to DAPI & analyzed relative to the control cultures. No groups were found to be significantly different by the Friedman test. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/32899433), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed) [NBP1-75617] -
Immunocytochemistry/ Immunofluorescence: Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed) [NBP1-75617] - Mouse WAT-CM induces the expression of CD24 in mesenchymal MDA-MB-231 cells but does not affect the expression of vimentin. Representative images of MDA-MB-231 cells cultured with or without lean or obese subcutaneous or visceral WAT-CM & co-stained for vimentin, CD24, & DAPI (a); scale bar = 100 µM. (b) & (c) are the relative expression of the respective markers, mean ± SEM (n = 6 biological replicates). The average protein expression from five images per replicate were normalized to DAPI & analyzed relative to the control cultures. Significance was determined by Friedman’s test. If significant, Dunn’s test was used for further pairwise comparison; * p < 0.05. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/32899433), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed) [NBP1-75617] -
Immunocytochemistry/ Immunofluorescence: Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed) [NBP1-75617] - Mouse WAT-CM induces the expression of epithelial biomarkers in mesenchymal triple negative breast cancer cell line grown in a 3D culture. (a) Representative images of MDA-MB-231 cells cultured with or without lean or obese subcutaneous or visceral WAT-CM & co-stained for E-cadherin, claudin-7, & DAPI; scale bar = 100 µm. (b) & (c) are the relative expression of the respective markers, mean ± SEM (n = 6 biological replicates). The average protein expression from five images per replicate were normalized to DAPI & analyzed relative to the control cultures. Significance was determined by the Friedman test. If significant, Dunn’s test was used for further pairwise comparison; * p < 0.05. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/32899433), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications
Flow Cytometry
Immunomicroscopy
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- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
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Background: IgG (H+L)
The 4 IgG subclasses, sharing 95% amino acid identity, include IgG1, IgG2, IgG3, and IgG4 for humans and IgG1, IgG2a, IgG2b, and IgG3 for mice. The relative abundance of each human subclass is 60% for IgG1, 32% for IgG2, 4% for IgG3, and 4% for IgG4. In an IgG deficiency, there may be a shortage of one or more subclasses (4).
References
1. Painter RH. (1998) Encyclopedia of Immunology (Second Edition). Elsevier. 1208-1211
2. Chapter 9 - Antibodies. (2012) Immunology for Pharmacy. Mosby 70-78
3. Schroeder H, Cavacini, L. (2010) Structure and Function of Immunoglobulins. J Allergy Clin Immunol. 125(2 0 2): S41-S52. PMID: 20176268
4. Vidarsson G, Dekkers G, Rispens T. (2014) IgG subclasses and allotypes: from structure to effector functions. Front Immunol. 5:520. PMID: 25368619
Additional IgG (H+L) Products
Product Documents
Certificate of Analysis
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Product Specific Notices
DyLight (R) is a trademark of Thermo Fisher Scientific Inc. and its subsidiaries.
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Secondary Antibodies are guaranteed for 1 year from date of receipt.
Citations for Donkey anti-Mouse IgG (H+L) Secondary Antibody [DyLight 594] (Pre-adsorbed)
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- 7-Amino Actinomycin D (7-AAD) Cell Viability Flow Cytometry Protocol
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Extracellular Membrane Flow Cytometry Protocol
- Flow Cytometry Protocol for Cell Surface Markers
- Flow Cytometry Protocol for Staining Membrane Associated Proteins
- Flow Cytometry Staining Protocols
- Flow Cytometry Troubleshooting Guide
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Intracellular Flow Cytometry Protocol Using Alcohol (Methanol)
- Intracellular Flow Cytometry Protocol Using Detergents
- Intracellular Nuclear Staining Flow Cytometry Protocol Using Detergents
- Intracellular Staining Flow Cytometry Protocol Using Alcohol Permeabilization
- Intracellular Staining Flow Cytometry Protocol Using Detergents to Permeabilize Cells
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Propidium Iodide Cell Viability Flow Cytometry Protocol
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Liperfluo
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Characterization of Human Th22 Cells
- Protocol for the Characterization of Human Th9 Cells
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- Troubleshooting Guide: Immunohistochemistry
- View all Protocols, Troubleshooting, Illustrated assays and Webinars