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CelRed nucleic acid gel stain 10,000× concentrate in water

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Catalog No. TD0002

CelRed nucleic acid gel stain 10,000× concentrate in water is a fluorescent dye used for nucleic acid staining, suitable for staining and detecting dsDNA, ssDNA, or RNA in agarose gels or polyacrylamide gels.

CelRed nucleic acid gel stain 10,000× concentrate in water

CelRed nucleic acid gel stain 10,000× concentrate in water

Copy Product Info
😃Good
Catalog No. TD0002
CelRed nucleic acid gel stain 10,000× concentrate in water is a fluorescent dye used for nucleic acid staining, suitable for staining and detecting dsDNA, ssDNA, or RNA in agarose gels or polyacrylamide gels.
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Product Introduction

Bioactivity
Description
CelRed nucleic acid gel stain 10,000× concentrate in water is a fluorescent dye used for nucleic acid staining, suitable for staining and detecting dsDNA, ssDNA, or RNA in agarose gels or polyacrylamide gels.
In vitro
When CelRed Stain is used to detect DNA by electrophoresis, it can be stained before electrophoresis (pre-staining, gel staining) or after electrophoresis (post-staining, bubble staining).
1. Gel staining method
1. Prepare agarose gel solution of appropriate concentration as needed.
2. After the agarose is completely dissolved and cooled appropriately, add CelRed Stain at a ratio of 5 μL dye per 100 mL gel solution (1×). After mixing, pour the agarose gel solution into the mold for preparing the gel.
3. After the gel solution solidifies, load the sample for electrophoresis according to the conventional method, and observe it under ultraviolet irradiation after the electrophoresis is completed.
Notes:
1. The gel staining method is not suitable for prefabricated polyacrylamide gels. For polyacrylamide gels, please use the bubble staining method.
2. CelRed Stain has good thermal stability and can be added directly to the hot agarose gel solution without waiting for the gel solution to cool.
3. CelRed Stain can be pre-mixed with the electrophoresis buffer containing agarose powder and heated to make gel.

2. Foam staining method
1. Perform electrophoresis according to the conventional method, and do not add any dye when making the gel.
2. Dilute CelRed Stain about 3,300 times into 0.1 M NaCl to make 3× CelRed Stain staining solution (for example, add 30 μL CelRed Stain to 100 mL 0.1 M NaCl solution).
3. Immerse the gel completely in 3× CelRed Stain staining solution and stain it for 30 minutes at room temperature in the dark. The staining time is determined by the gel concentration and thickness. The thicker the gel and the higher the concentration, the longer the staining time required.
4. After staining, it can be observed under ultraviolet light.
Notes:
1. 3× CelRed Stain staining solution can be prepared in large quantities and needs to be stored in the dark at room temperature.
2. When staining by the foam staining method, the amount of dye used is large, and a single use of 3× CelRed Stain staining solution can be reused about 3 times.

The above information is based on published literature. Experimental procedures should be appropriately modified to meet specific research demands.
Chemical Properties
Relative Density.no data available
Storage & Solubility Information
Storagekeep away from direct sunlight | store at -20°C | Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
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Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
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2 Enter the in vivo formulation:
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