Lablead

Prix FOB

Obtenir le dernier prix

- Minimum Order

Pays:

China

N Â° de modÃ¨le:

Prix FOB:

(Negotiable) Obtenir le dernier prix

LocalitÃ©:

China

Prix de commande minimale:

Commande minimale:

Packaging Detail:

Heure de livraison:

7-15 days if in stock

Capacité de Fournir:

Payment Type:

T/T, L/C, D/A, D/P, Western Union, Money Gram, PayPal, Other

Groupe de produits :

Molecular Biology

Contacter maintenant

Lablead biotech

China

200 Points de confiance

1st Année

Personne Ã contacter Ying

Contacter maintenant

SpÃ©cification du produit

La description

CelRed Nucleic acid dye

CATï¼šCR**1

Price:U.S.ï¼„*0.*0 for **0ul (negotiable if bulk purchase)

Product IDï¼šCR******0uL Storageï¼šStore for *4 months at room temperature and away from light. CelRed Nucleic acid dye features Non-toxic: CelRed's unique oiliness and large molecular weight make it unable to penetrate the cell membrane into the cell, and Ames' test results also show that the mutagenicity of the dye is much less than EB.
High sensitivity: suitable for electrophoretic staining of fragments of various sizes, the effect on nucleic acid migration is less than that of SYBR Green I.
High stability: suitable for using microwave or other heating methods to prepare agarose gel; Extremely stable in acid or alkali buffers at room temperature, strong light resistance.
High signal-to-noise ratio: the fluorescence signal of the sample is strong, the background signal is low.
Simple operation: Like EB, the dye does not degrade during the preforming and electrophoresis process; The dyeing process after electrophoresis also takes only *0 minutes without decolorization or rinsing, and can be directly observed with the ultraviolet gel transmisometer.
Wide range of application: you can choose pre-electrophoresis dyeing (glue dyeing) or post-electrophoresis dyeing (bubble dyeing); Suitable for agarose gel or polyacrylamide gel electrophoresis; Can be used for dsDNA, ssDNA or RNA staining.
It has the same spectral characteristics as EB, no need to change the filter and observation device: Standard EB filter or SYBR filter is suitable, using the same ordinary UV gel transmisometer as EB observation can be observed, and the best excitation can be obtained near **0nm UV light. However, CelRed cannot be fully excited by **8 nm argon-ion lasers or visible light of similar wavelengths, so imaging systems using such excitation devices are not recommended.
Introduction to using CelRed
1. Glue dyeing method (same as EB) (recommended method)
(1) Add CelRed nucleic acid dye when making glue (for example: add 5μL CelRed *0,**0× storage solution per *0mL agarose solution, and so on).
(2) Electrophoresis was performed according to conventional methods.
Note:
The amount of dye used in this method is relatively small. **0 μL of dye can make about **0 pieces of *0mL glue.
Because CelRed has good thermal stability, it can be added directly in a hot agarose solution without waiting for the solution to cool. Shake, oscillate, or flip to ensure that the dye is well mixed. Alternatively, the CelRed reservoir can be added to the agarose powder and electrophoresis buffer, and then heated in the microwave or other common method to prepare the agarose gel. CelRed is compatible with all commonly used electrophoresis buffer solutions.
If you always see band dispersion or separation is not ideal, it is recommended to use bubble dyeing to confirm whether the problem is related to the dye. If the problem persists after dyeing, the problem is not related to the dye, please try: reduce the agarose concentration; Use longer gels; Extend the gel time to ensure clear edges; Improve the sampling technique or choose blister dyeing method.
This method is not suitable for prefabricated polyacrylamide gel, please use the foam dyeing method for polyacrylamide gel.

2. Blister dyeing
(1) Electrophoresis was performed according to conventional methods.
(2) The CelRed *0,**0× storage solution was diluted about 3,**0 times with H2O into 0.1M NaCl to make a 3× dyeing solution. (For example, add *5μL CelRed *0,**0× reservoir and 5mL 1M NaCl to *5mL H2O).
(3) Place the gel carefully into a suitable container, such as a polypropylene container. Slowly add a sufficient amount of 3× dye solution to immerse the gel. The optimal dyeing time varies slightly according to the gel thickness and agarose concentration. For gels containing 3.***0% acrylamide, the dyeing time is usually between *0min and 1h, and increases with the increase of acrylamide content.
(4) The results were observed by a **2nm stimulated UV gel imaging system.
Note:
When dyeing with bubble dyeing method, the amount of dye is more. A single use of the dye solution can be reused for about 3 times.
3×CelRed dyeing solution can be prepared in large quantities and stored away from light at room temperature until used up.
3. PAGE steps for nucleic acid electrophoresis:
(1) Put the gel prepared by TBE into the electrophoresis tank and hold the edge with a clamp.
(2) Fill the buffer tank with 5×TBE in the same batch as the gel solution. Use a syringe to remove air bubbles from the bottom of the gel.
(3) Use a syringe to draw 1×TBE to flush the sample addition hole. The DNA sample was mixed with an appropriate amount of 6× gel loading buffer, and added into the sampling hole with a micro-pipette.
(4) Connect the electrode to the power supply (positive terminal slot), turn on the power supply generally *0V; 1 to 8V/cm. Electrophoresis was performed for 9h.
(5) Electrophoresis until the standard reference dye migrates to the desired position (generally, electrophoresis until the xylene is completely removed, and the bromophenol blue is stopped 2 ~ *5px from the bottom edge). Turn off the power, unplug and discard the electrophoresis solution from the bath.
(6) Take the gel off and put it in the dyeing dish, add 3XCelRed 1X buffer for oscillating dyeing for ****0 minutes, and place it in the ultraviolet detection.
Note:
PAGE glue is different from aglyceride sugar gel, which can not be pre-dyed or spot-dyed. Can only use foam dyeing method color, because polyacrylamide is relatively dense, the dye is not easy to go deep, the color effect is not as good as Joan ester sugar gel.
Special reminder:
If you are using an ultraviolet imager, choose CelRed; If you use a laser imager or wish to observe in visible light, choose CelGreenï¼ˆCATï¼šCG**1ï¼‰.
In rare cases where the DNA sample after the plasmid has been cut by certain enzymes has a tailing and reduced resolution, it is recommended to try both staining methods to determine which is more appropriate.

Pays:	China
N Â° de modÃ¨le:	-
Prix FOB:	(Negotiable) Obtenir le dernier prix
LocalitÃ©:	China
Prix de commande minimale:	-
Commande minimale:	-
Packaging Detail:	-
Heure de livraison:	7-15 days if in stock
Capacité de Fournir:	-
Payment Type:	T/T, L/C, D/A, D/P, Western Union, Money Gram, PayPal, Other
Groupe de produits :	Molecular Biology