BIO RAD 200/2.0 Bedienerhandbuch

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Trans-Blot
®
SD
Semi-Dry
Electrophoretic
Transfer Cell
Instruction
Manual
Catalog Number
170-3940
For Technical Service Call Your Local Bio-Rad Office or in the U.S. Call 1-800-4BIORAD (1-800-424-6723)
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Inhaltsverzeichnis

Seite 1 - 170-3940

Trans-Blot®SDSemi-DryElectrophoreticTransfer CellInstructionManualCatalog Number170-3940For Technical Service Call Your Local Bio-Rad Office or in the

Seite 2 - Warranty

Low molecular weight macromolecules ( 10,000 daltons) may diffuse out of gels morereadily. One can allow adequate gel pre-equilibration by changing th

Seite 3 - Table of Contents

2. Place a pre-soaked sheet of extra thick filter paper onto the platinum anode. Roll a pipetor test tube over the surface of the filter paper (like a

Seite 4 - Introduction

7. Carefully place the cathode onto the stack. Press to engage the latches with the guideposts without disturbing the filter paper stack.8. Place the

Seite 5 - Equipment and Reagents

4.3 Assembly of the Unit for Acidic TransfersIf an acidic transfer buffer is used, the transfer direction will be from the anode to thecathode.1. Rem

Seite 6

Note: Some pH electrodes will not perform a proper measurement for the pH of Trisbuffers. If the pH of the buffer is not correct, check the electrode

Seite 7 - 2.3 Chemical Reagents

6.2 DNA Blotting(For acrylamide gels with DNA 250 bp to ~1 kb)Electrophoresis Run on a Polyacrylamide Gel1. Prepare the stock electrophoresis 5x TBE

Seite 8 - Safety Instructions

Nitrocellulose membranes have been used extensively for protein binding and detec-tion.7,19-22They can easily be stained for total protein by a dye st

Seite 9 - Trans-Blot SD Assembly

6. Methanol in the transfer buffer is restricting elution of proteins from the gel. Eliminationof methanol results in increased transfer efficiency, b

Seite 10

8.4 Poor Detection Sensitivity or No Reactivity1. Consult detection kit manual.2. Antigen binding is incomplete. See Troubleshooting Sections 8.1–8.3

Seite 11

Life ScienceGroupWebsite www.bio-rad.com Bio-Rad Laboratories Main Office 2000 Alfred Nobel Drive, Hercules, CA 94547, Ph. (510) 741-1000, Fx. (510)7

Seite 12

NoteTo insure the best performance from the Trans-Blot SD semi-dry electrophoretic transfercell, become fully acquainted with these operating instruct

Seite 13 - Buffer Formulation

Table of ContentsPageSection 1 Introduction... 11.1 Sp

Seite 14 - Section 6

Section 1IntroductionBlotting was first performed by Southern1in 1975 with the transfer of DNA from agarosegels to nitrocellulose membranes. Blotting

Seite 15 - Section 7

Section 2Equipment and Reagents2.1 Equipment and AccessoriesCatalogNumber Product Description170-3940 Trans-Blot SD Electrophoretic Transfer CellRepl

Seite 16 - Troubleshooting Guide

CatalogNumber Product DescriptionNitrocellulose Membrane (0.2 micron) Recommended uses162-0112 Roll, 33 cm x 3 m, 1162-0146 Sheets, 7 x 8.4, 10162-014

Seite 17

2.2 Related InstrumentsCatalogNumber Product DescriptionBlotting Equipment170-3910 Trans-Blot Electrophoretic Transfer Cell170-3946 Trans-Blot Electr

Seite 18 - Section 9

CatalogNumber Product DescriptionTotal Protein Detection Kits170-6512 Biotin-Blot Protein Detection Kit170-6517 Enhanced Colloidal Gold Total Protein

Seite 19 - Laboratories

4. Lengthy transfer times are not recommended. Do not leave this instrument unattended.Joule heat can be generated rapidly during semi-dry blotting. T

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