additional PIC did not substantially alter the results Using this method we have obtained much improved 1D and 2D GE results for root or root and leaf tissue in terms of number and intensity of protein band/spots Raorane and Kohli unpublished results Success of such a simple but efficient method using Tris buffer depends on the type of
Get PriceImmediately transfer pulverized tissue with the help of a frozen spatula to a ml tube containing 1 ml of extraction buffer vortex for 15 s and then incubate on ice for 5 min v Add 200 µl of chloroform and vortex thoroughly for 15 s then incubate on ice for 10 min Centrifuge it for 5 min at 12000×g at 4°C vi
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Get PricePigments were extracted by crushing 1g of petals in 1mL of solvent with the use of a mortar and pestle The slurry generated were transferred into 1 5mL Eppendorf tubes and vortexed Fisher Vortex Genie 2TM from Fisher Scientific for 10mins for maximum extraction of the pigments The resultant mixtures were then centrifuged Eppendorf Centrifuge Model no 5415D at 11 000RPM for 30mins to
Get Price24 Dispense 100 l of TE buffer and completely dissolve it by using a vortex 25 Pour the mixture into a tube and store it in a freezer Dec 2024 Highspeed micro centrifuge CF15RXII /CF16RXII / T15A45 fixed angle rotor Extraction of Genomic DNA from Rice Leaf by using a 5ml 2024
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Get PriceOur study suggested that grinding of date palm leaf with sterile sand and inclusion of NaCl M in the lysis buffer without the costly use of liquid nitrogen PVP and LiCl provides a DNA yield of sufficient purity suitable for PCR amplification Keywords DNA extraction PCR plants tough leaves date palm Phoenix dactylifera 1 Introduction Most of the plant DNA isolation methods
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Get PriceSoak the leaf discs in the solution for 2 min and shake the plate gently to sterilize the leaf surface 6 Remove the sterilization solution and wash the leaf discs twice with mL of sterile water 7 Dry the leaf discs on a clean surface under the laminar flow cabinet for 20 30 min 8 Add 3 metal beads in each mL Eppendorf safe lock
Get PriceNeonate larvae 8 per plant were allowed to feed for days Control plants were caged without insects Electrical signals were monitored on the petiole of leaf 13 after mechanically crush wounding leaf 8 Data are means ± SD n = 7 8 biological replicates B Time course for the effect of S littoralis feeding on surface potentials At
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Get PriceA quick DNA extraction from kanamycin resistant seedling was obtained by crushing one leaf with plastic rod directly against microtube wall containing 300 μL of EB buffer 200 mM Tris HCl 25 mM EDTA 250 mM NaCl % SDS When the solution turned transparent green 100 μL of Cloroform was added and shaken for 1 min using Vortex
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Get PriceApproximately 20 mg of freeze dried ground leaf tissues were weighed into Eppendorf tubes Subsequently 500 μl of 100% methanol containing 4% internal standard from a stock solution containing mg ml −1 13 C 6 sorbitol/valine was added to the samples The samples were then shaken for 20 min at 30°C in a thermomixer at 21 100 g and subsequently centrifuged for 10 min at 4°C at 18
Get PriceIf the PCR test is to be used avoid carry over of DNA on containers or grinding apparatus Crushing in disposable bags and use of 1 mM EDTA [pH 8 0] into a 1 5 ml Eppendorf tube 2 Add 100 µl sample extract and place in a heating block or water bath at 95 °C for 10 min 3 Put tube on ice for 5 min 4 Add 80 µl Lysozyme stock solution 50 mg Lysozyme per ml in 10 mM Tris HCl pH 8 0
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Get PriceLeaf samples of grams pvp and liquid nitrogen were crushed in a mortar until they became powder Then put in an eppendorf tube that already contains the extraction buffer and then shaken Then homogenized using a vortex and incubated in a water bath at a temperature of 650C for 30 minutes
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Get Pricea The infected leaves were crushed to fine powder in liquid nitrogen using baked mortar and pestle b The tissue powder 100 mg was immediately transferred to an eppendorf containing 450 µl of RLT Buffer or RLC Buffer solution and vortex vigorously c The homogenate was incubated at 56C for 1 3 min which help to disrupt the tissue
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