Bio-rad ReadyPrep™ 2-D Starter Kit Bedienungsanleitung

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ReadyPrep
2-D Starter Kit
Instruction Manual
Catalog Number
163-2105
For technical service
call your local Bio-Rad office or
in the U.S. call 1-800-4BIORAD
(1-800-424-6723)
On the Web at http://www.discover.bio-rad.com
Seitenansicht 0
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Inhaltsverzeichnis

Seite 1 - 2-D Starter Kit

ReadyPrep™2-D Starter KitInstruction ManualCatalog Number163-2105For technical servicecall your local Bio-Rad office orin the U.S. call 1-800-4BIORAD(

Seite 2 - Table of Contents

4 Overlay each of the strips with 2 to 3ml of mineral oil to prevent evaporationduring the rehydration process. Addthe mineral oil slowly, by carefull

Seite 3 - Kit Components

9Fig. 6 Wetting the electrode wicks with water.Fig. 7 Draining the oil. Fig. 8 Placing the ReadyStrip gel side downin the focusing tray.

Seite 4 - Section 3

Draining the oil essentially washes theoutside surface of the gel, removingunabsorbed protein and resulting inreduced horizontal streaking. If desired

Seite 5 - Instructions for Use

4.4 Completion of IEF.1. When the electrophoresis run has been completed, remove the IPG strips from the focus-ing tray and transfer them gel side up

Seite 6 - 7 cm 11 cm 17 cm

6 Figure 9 shows the expected pattern when IPG strips of 17 cm, 11 cm, and 7 cm arestained with IEF gel staining solution (catalog # 161-0434) and des

Seite 7

a Remove the kit from the refrigerator and unpack the 2 bottles of equilibration buffer I (WHITE or SILVER caps), the 2 bottles of equilibration buffe

Seite 8

6. Using Table 3, add the indicated volume of complete equilibration buffer II (containingiodoacetamide) to each strip.7. Return the tray to the orbit

Seite 9

3. Remove an IPG strip from the disposable rehydration/equilibration tray and dip briefly intothe graduated cylinder containing the 1X Tris/glycine/SD

Seite 10

5 Using the forceps, carefully push the strip into the well as shown in Figure 13, taking carenot to trap any air bubbles beneath the strip. When push

Seite 11

174.9 STAINING.The 2-D starter kit was designed so that sufficient protein sample loaded in the IEFdimension readily stain second-dimension SDS-PAGE g

Seite 12

Table of ContentsSection 1 Introduction ...1Section 2 Kit Components...

Seite 13

4.10 Imaging.1 To preserve the gel images, the destained gels can be imaged on a densitometer such asBio-Rad’s GS-800 calibrated imaging densitometer

Seite 14

19Fig. 14 C. PROTEAN Ready Gel stained with Bio-Safe stain.

Seite 15

20Figure 15 A. Ready Gel stained with Coomassie Blue R-250 stain.Fig. 15 B. Criterion stained with Coomassie Blue R-250 stain.

Seite 16

21Figure 15 C. PROTEAN Ready Gel stained with Coomassie Blue R-250 stain.

Seite 17

Section 5AppendixA Buffer and Reagent PreparationTo avoid introducing experimental error when using this kit, we suggest using premixed buffersand sta

Seite 18

234. - The first line displays the step number, slope and voltage- Select HRS:MIN (default)- Enter time of 20 min. - Press NEXTS 01 250 VHRS:MIN vhour

Seite 19

2411. - Select METHOD COMPLETEADD inset delete >ENTER STEP # >NEXT >METHOD COMPLETE >12. - The save method screen is displayed when the na

Seite 20 - 4.10 Imaging

Section 6Product InformationCatalogNumber Product Description2-D Starter Kit accessories163-2105 ReadyPrep 2-D Starter Kit163-2106 ReadyPrep Rehydrati

Seite 21

Bio-Rad Laboratories, Inc.2000 Alfred Nobel Dr., Hercules, CA 94547510-741-10004110009 Rev A

Seite 22

Section 1IntroductionThe ReadyPrep™2-D starter kit was designed as a single-use kit to familiarize first-time users withthe utilization of the Bio-Rad

Seite 23

Overlay Agarose. One bottle containing 50 ml of 0.5% low melting point agarose in 25 mMTris, 192 mM glycine, 0.1% SDS, and a trace of Bromophenol Blue

Seite 24 - Appendix

Section 4Instructions for UseIntroductionThis 2-D starter kit allows you to successfully separate a complex protein extract by 2-D PAGEusing IPG strip

Seite 25

4Rehydration Setup30 minRehydration Setup30 minIPG Rehydration12 hoursIPG Rehydration12 hoursIPG Rehydration12 hoursIsoelectric Focusing5 hoursIsoelec

Seite 26

4.1 Sample Preparation1 Remove the bottle of rehydration/sample buffer, the bottle of nanopure water and the vialof E. coli protein sample from the ki

Seite 27 - Product Information

2. Repeat this process for the remaining samples by pipetting the indicated volume of sample into adjacent channels. It is best to place samples on bo

Seite 28 - Bio-Rad Laboratories, Inc

Gently place the strip gel side down onto the sample as illustrated in Figure 4. The “+”and “pH 4-7” should be legible and positioned at the left side

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