Bio-rad Aurum™ Total RNA 96 Kit Uživatelský manuál

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Strany 1 - Total RNA 96 Kit

Catalog #732-6800Aurum™ Total RNA 96 Kit Instruction Manual

Strany 2

6 Disruption and Homogenization Proper disruption and homogenization of the starting materials are required to ensure complete lysis of the cells an

Strany 3 - Table of Contents

7 Preparing the Aurum™ Vacuum Manifold Tubing provided in the Aurum™ Vacuum Manifold kit is 4 ft long and must be cut into appropriate pieces before

Strany 4

8 2. Place the desired 96-well binding plate on the manifold top and apply the recommended vacuum pressure for your application. Manifold Elution

Strany 5 - Kit Components

9 Section 7 Vacuum Protocol PleasereadSection5,“BeforeUsingtheAurum™TotalRNA96Kit”andSection 6, “Vacuum Manifold Setup and Use With 96-

Strany 6 - Necessary Supplies

10 Yeast Follow steps C1–C5, then continue with step 1 of “All Starting Cell Types” onpage10.Ifstartingwithagrowblockofyeastculture(max

Strany 7 - Total RNA 96 Kit

11 5. Add700µloflowstringencywashsolutiontoeachwelloftheRNAbinding plate. Gradually increase the negative pressure between –17 to –23

Strany 8 - S. cerevisiae

12 Note: Gradual application of negative pressure is required to prevent sample spraying and cross-contamination. The eluted total RNA sample

Strany 9

13B2. Add350µloflysissolution(alreadysupplementedwith 1%b-mercaptoethanol) to each sample and pipet up and down several times to mix thoro

Strany 10 - 96-Well Plates

14 5. Add700µloflowstringencywashsolutiontoeachwelloftheRNAbinding plate. Centrifuge for 2 min at 1,500 x g. Discard the low stringen

Strany 11 - Vacuum manifold

15 Section 9 Troubleshooting Guide Problem Possible Cause Recommended Solution Difficulty achieving Purge step in protocol If sealing of well

Strany 13 - Vacuum Protocol

16 Problem Possible Cause Recommended Solution Low or highly variable Elution solution applied Apply elution solution eluate volumes among to

Strany 14

17 Problem Possible Cause Recommended Solution Clogging of RNA Excessive amount of Reduce volume of binding plate starting material per well

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18 Problem Possible Cause Recommended Solution Total RNA prep Incorrect use of wash Add the appropriate performs poorly in  solutions volum

Strany 16 - Spin Protocol

19 Section 10 OrderingInformation Catalog # Description 732-6800 Aurum™ Total RNA 96 Kit 732-6470 Aurum™ Vacuum Manifold 732-6820 Aurum™

Strany 17

Bio-Rad Laboratories, Inc. 2000 Alfred Nobel Dr. Hercules, CA 94547 USA (510) 741-1000 1-800-424-6723 Life ScienceGroup10-1554 1210 Sig 111

Strany 18

Table of Contents Section 1 Introduction...1 Section 2 Kit Components ...1 Section 3 Storage

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Section 1 Introduction The Aurum™ Total RNA 96 kit rapidly purifies up to 192 total RNA samples from biological samples (e.g. mammalian cells, yea

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Section 3 Storage Conditions All kit components (including lyophilized DNase I) should be stored at room temperature. Store reconstituted DNase I

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Section 5 BeforeUsingthe Aurum™ Total RNA 96 Kit Please read the following guidelines before proceeding with the total RNA purification. Start

Strany 23 - OrderingInformation

Table 1. Yield (per well) of total RNA from various samples using the Aurum™ Total RNA 96 kit. Starting Material Avg. Yield (µg)* Cultured cell

Strany 24 - 1-800-424-6723

• Vendors of lyticase, which is used to partially degrade the cell walls of yeast cells, may have different definitions of the enzyme’s activity.

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