Promega AS1380 Maxwell RSC simplyRNA Blood Kit Instruction Manual
- June 5, 2024
- Promega
Table of Contents
- Promega AS1380 Maxwell RSC simplyRNA Blood Ki
- Description
- Description (continued)
- Product Components and Storage Conditions
- Product Components and Storage Conditions (continued) For Manual
- Preparation of Solutions
- Maxwell® RSC simplyRNA Blood Cartridge Preparation
- Maxprep™ Preprocessing
- Maxprep™ Cartridge Preparation (continued)
- Maxprep™ Liquid Handler Preprocessing Protocol
- Maxwell® Instrument Setup and Run
- Storing Eluted RNA
- Troubleshooting
- Causes and Comments
- Appendix
- Related Products Instrument and Accessories
- References
- Read User Manual Online (PDF format)
- Download This Manual (PDF format)
Promega AS1380 Maxwell RSC simplyRNA Blood Ki
Description
The Maxwell® RSC simplyRNA Blood Kit (a) is designed for isolation of total
RNA from fresh (not frozen) whole blood collected in EDTA tubes. The simplyRNA
Blood procedure purifies total RNA with minimal sample handling before
automated purification on the Maxwell® RSC Instrument or Maxwell® RSC 48
Instrument. The Maxwell® RSC and Maxwell® RSC 48 Instruments are supplied with
preprogrammed purification procedures and are designed for use with
predispensed reagent cartridges, maximizing simplicity and convenience. The
Maxwell® RSC Instrument can process up to 16 samples, and the Maxwell® RSC 48
Instrument can process up to 48 samples in about 50 minutes. The low elution
volume results in concentrated high-quality RNA suitable for use in downstream
applications such as quantitative
RT-PCR (qRT-PCR).
Description (continued)
The Maxwell® RSC simplyRNA Blood Kit purifies samples using a paramagnetic
particle that provides a mobile solid phase that optimizes sample capture,
washing and purification of nucleic acid. The Maxwell® RSC and Maxwell® RSC 48
Instruments are magnetic particle-handling instruments that efficiently bind
RNA to the paramagnetic particle in the first well of a prefilled cartridge.
The samples are processed through a series of washes before the RNA is eluted.
Prior to extraction, samples can be preprocessed manually or using the
Maxprep™ Liquid Handler. The Maxprep™ Liquid Handler will transfer samples
from primary sample tubes, perform sample lysis prior to extraction, add lysed
samples to Maxwell® RSC cartridges, transfer plungers to Maxwell® RSC
cartridges, and dispense elution buffer to elution tubes. Follow the
instruction set specific to the preprocessing option used.
Product Components and Storage Conditions
Maxwell® RSC simply RNA Blood Kit
For Research Use. Sufficient for 48 automated isolations from fresh blood in EDTA collection tubes. Cartridges are single-use only. Includes:
- 4 × 100ml Cell Lysis Solution
- 30ml Homogenization Solution
- 20ml Lysis Buffer
- 2 × 1ml Proteinase K
- 900µl 1-Thioglycerol
- 2 vials DNase I (lyophilized)
- 50µl Blue Dye
- 48 Maxwell® RSC Cartridges
- 1 Maxwell® RSC Plunger Pack (48 Plungers)
- 50 Elution Tubes, 0.5ml
- 25ml Nuclease-Free Water
Maxwell® RSC simply RNA Blood Kit Multi-Pack
For Research Use. Not for use in diagnostic procedures. Each Multi-Pack
contains sufficient reagents for 144 automated isolations. Cartridges are
single-use only. Note: ASB1380 is not recommended for use with the Maxprep™
Liquid Handler. Includes:
- 12 × 100ml Cell Lysis Solution
- 3 × 30ml Homogenization Solution
- 3 × 20ml Lysis Buffer
- 6 × 1ml Proteinase K
- 3 × 900µl 1-Thioglycerol
- 6 vials DNase I (lyophilized)
- 3 × 50µl Blue Dye
- 144 Maxwell® RSC Cartridges
- 3 × 50/pk RSC/CSC Plungers
- 3 × 50 Elution Tubes, 0.5ml
- 3 × 25ml Nuclease-Free Water
Storage Conditions: Upon receipt, remove the 1-Thioglycerol and store at
+2°C to +10°C. Store the remaining
kit components at room temperature (+15°C to +30°C). 1-Thioglycerol also can
be stored at room temperature
(+15°C to +30°C), where it is stable for up to 9 months.
Safety Information: The Maxwell® RSC Cartridges contain ethanol, which is
flammable and an irritant. 1-Thioglycerol is toxic. Guanidine thiocyanate and
guanidine hydrochloride (which are components of the Homogenization Solution
and Lysis Buffer) are toxic, harmful and irritants. Wear gloves and follow
standard safety procedures while working with these substances. Refer to the
SDS for detailed safety information.
Caution: The Maxwell® RSC Cartridges are designed to be used with
potentially infectious substances. Wear appropriate protection (e.g., gloves
and goggles) when handling infectious substances. Adhere to your institutional
guidelines for the handling and disposal of all infectious substances used
with this system.
Caution: Handle cartridges with care; seal edges may be sharp. Bleach
reacts with guanidine thiocyanate and should not be added to any sample waste
from these cartridges.
Product Components and Storage Conditions (continued) For Manual
Preprocessing
For Manual Preprocessing PR ODUC T| SIZE|
CAT. #
---|---|---
Cell Lysis Solution| 1L| A7933
For Preprocessing with the Maxprep™ Liquid
Handler
**PR ODUC T**
| SIZE| CAT. #
Maxprep™ 1000µl Conductive Disposable Tips, Filtered| 40/box|
AS9303
Maxprep™ 300µl Conductive Disposable Tips, Filtered| 60/box|
AS9302
Maxprep™ Reagent Reservoir, 50ml| 28/pack| AS9304
Maxwell® RSC Plunger Pack| 48/pack| AS1670
Maxprep™ Plunger Holder| 1 each| AS9408
Maxprep™ 3-Position Reagent Tube Holder| 1 each| AS9409
3. Sample Preparation
| |
Sample Preparation
! The Maxwell® RSC simplyRNA Blood Kit can process 2.5ml of fresh whole blood per RNA isolation.
Preparation of Solutions
Mixture of 1-Thioglycerol and Homogenization Solution
A volume of 200µl of 1-Thioglycerol/Homogenization Solution mixture is needed
for each sample. To prepare a working solution, add 20µl of 1-Thioglycerol per
milliliter of Homogenization Solution. 1-Thioglycerol is viscous, so careful
pipetting is required for accurate measurement. Alternatively, add 600µl of
1-Thioglycerol to the 30ml bottle of Homogenization Solution. Before use,
chill the mixture of 1-Thioglycerol and Homogenization Solution on ice or at
+2°C to +10°C.
Note: Store the mixture of 1-Thioglycerol and Homogenization Solution at
+2°C to +10°C, where it is stable for up to 30 days.
DNase I Solution
Add 275µl of Nuclease-Free Water to the vial of lyophilized DNase I. Invert to
rinse DNase off the underside of the cap, and swirl gently to mix; do not
vortex. Add 5µl of Blue Dye to the reconstituted DNase I as a visual aid for
pipetting. Dispense the DNase I Solution into single-use aliquots in 1.5ml
nuclease-free tubes (such as ClickFit Microtubes, Cat.# V4741). Each
purification requires 10µl of DNase I solution. Store reconstituted DNase I at
–30°C to –10°C. DNase I solution maintains activity for up to 10 freeze-thaw
cycles.
Preparing White Blood Cell Pellets Materials to Be Supplied By the User
- fresh (not frozen) whole blood in EDTA collection tubes
- benchtop vortex mixer
- 14ml tubes and caps (sterile; e.g., Corning Cat.# 352006)
- centrifuge with swinging-bucket rotor
- RNase-free, sterile, aerosol-resistant pipette tips
Note: The Maxwell® RSC simplyRNA Blood Kit contains two reagents with the word lysis in their name: Cell Lysis Solution (Part# A793A, 100ml) and Lysis Buffer (Part# MC501C, 20ml). Please check that you use the correct reagent at each step.
-
Transfer 2.5ml of well-mixed fresh (not frozen) whole blood from the EDTA collection tube into a sterile
14ml tube. -
Add 7.5ml of Cell Lysis Solution (Part# A793A), and invert the tube 5–6 times to mix. This is a differential lysis step; the red blood cells are lysed, leaving the white blood cells intact.
-
Incubate lysates for 10 minutes at room temperature. Twice during the incubation, invert to mix.
-
Centrifuge tube at 3,000 × g for 10 minutes.
-
Remove and discard as much of the supernatant as possible without disturbing the visible white pellet. Briefly spin to collect residual liquid at the bottom of the tube, and remove and discard the supernatant with a pipette.
-
Add 200µl of chilled 1-Thioglycerol/Homogenization Solution mixture to the pellet. Mix well with a pipette or vortex or both to ensure complete resuspension of the pellet.
Manual Preprocessing Materials to Be Supplied By the User
- benchtop vortex mixer
- RNase-free, sterile, aerosol-resistant pipette tips
Preprocessing of Lysed White Blood Cell Pellets
- Add 200µl of Lysis Buffer (Part# MC501C) and 25µl of Proteinase K to the resuspended white blood cell pellet. Mix by vortexing for 20 seconds.
- Incubate at room temperature for 10 minutes. During this time, prepare cartridges as described in Section 4.B.
- Add 10µl of blue DNase I Solution (prepared as described in Section 3.A) to well #4 of the Maxwell® RSC simply RNA Blood Cartridge (well #4 contains yellow reagent). After the blue DNase I Solution is added, the reagent in well #4 will be green.
- Add lysate to well #1 (the largest well) of the Maxwell® simply RNA Blood Cartridge.
- Proceed to Section 6, Maxwell® Instrument Setup and Run.
Maxwell® RSC simplyRNA Blood Cartridge Preparation
Cartridges should be prepared shortly before adding the lysate at Step 4 in Section 4.A.
-
To maintain an RNase-free environment during processing, change gloves before handling Maxwell® RSC Cartridges, RSC Plungers and Elution Tubes (0.5ml). Place the cartridges to be used in the deck tray(s) with well #1 (the largest well in the cartridge) facing away from the elution tubes. Press down on the cartridge to snap it into position. Carefully peel back the seal so that all plastic comes off the top of the cartridge. Ensure that all sealing tape and any residual adhesive has been removed before placing cartridges in the instrument
-
Place one plunger into well #8 of each cartridge.
-
Place an empty elution tube into the elution tube position for each cartridge in the deck tray.
-
Add 50μl of Nuclease-Free Water to the bottom of each elution tube.
Notes: -
Specimen or reagent spills on any part of the deck tray should be cleaned with a detergent-water solution, followed by a bacteriocidal spray or wipe, and then water. Do not use bleach on any instrument parts.
-
Use only the 0.5ml Elution Tubes provided in the kit; other tubes may be incompatible with the Maxwell® Instrument.
User Adds to Wells
- Preprocessed samples
- DNase I SolutionQ
- RSC Plunger
Figure 1. Maxwell® RSC Cartridge. Figure 2. Setup and configuration of the deck tray(s). Nuclease-Free Water is added to the elution tubes as shown. Plungers are in well #8 of the cartridge.
Maxprep™ Preprocessing
Maxprep™ Preprocessing
- Turn on the Maxprep™ Liquid Handler and PC. Log in to the PC, and start the Maxprep™ software on the PC by double-clicking the desktop icon.
- Touch Start to access the ‘Methods’ screen.
- On the ‘Methods’ screen, select a method using one of the two options below:
- Touch the simplyRNA Blood preprocessing method or laboratory-specific variant of the simplyRNA Blood preprocessing method.
- Use a bar code reader to scan the 2D bar code on the kit box to automatically select the appropriate base method. Touch the laboratory-specific variant of the simplyRNA Blood preprocessing method if desired.
- Verify that the appropriate preprocessing method or variant method has been selected, and touch the Proceed button. Close the instrument door and touch the Run button on the method run screen to start the run.
- Enter any method-specific variables (Sample Number, Elution Volume).
- Before placing Maxwell® RSC or Maxwell® RSC 48 deck tray(s) on the instrument, prepare the deck tray(s) with cartridges and elution tubes. Change gloves before handling Maxwell® RSC Cartridges, RSC Plungers and Elution Tubes (0.5ml). Place the cartridges to be used in the deck tray(s) with well #1 (the largest well in the cartridge) facing away from the elution tubes. Press down on the cartridge to snap it into position. Carefully peel back the seal so that all plastic comes off the top of the cartridge. Ensure that all sealing tape and any residual adhesive are removed before placing cartridges in the instrument. Place an empty elution tube into the elution tube position for each cartridge in the deck tray(s).
Notes:
- Specimen or reagent spills on any part of the deck tray should be cleaned with a detergent-water solution, followed by a bacteriocidal spray or wipe, and then water. Do not use bleach on any instrument parts.
- Use only the 0.5ml Elution Tubes provided in the kit; other tubes may be incompatible with the Maxwell® Instrument.
Maxprep™ Cartridge Preparation (continued)
Follow instrument setup instructions displayed in the method. You will be directed by the Maxprep™ software where to place the following items on the instrument:
Labware Type
-
Maxprep™ Plunger Holders with Maxwell® RSC Plunger Packs (2; one may be partially full)
-
Maxwell® RSC 48 Front deck tray or Maxwell® RSC deck tray containing Maxwell® RSC cartridges with seals removed and open elution tubes
-
Maxwell® RSC 48 Back deck tray or Maxwell® RSC deck tray containing Maxwell® RSC cartridges with seals removed and open elution tubes (depending on sample number)
-
Maxprep™ 3-Position Reagent Tube Holder with up to 3 tubes containing Proteinase K
-
Maxprep™ 3-Position Reagent Tube Holder with up to 3 tubes containing DNase I Solution
-
Maxprep™ Reagent Reservoir, 50ml with Lysis Buffer
-
Maxprep™ Reagent Reservoir, 50ml with Nuclease-Free Water
-
tube carriers loaded with tubes containing white blood cell lysates. All tubes within a carrier must be of the same type.
Note: Do not place 15ml conical tubes on the instrument; tips will crash into the tubes. -
Maxprep™ 1000µl Conductive Disposable Tips, Filtered (2; one may be partially full)
-
Maxprep™ 300µl Conductive Disposable Tips, Filtered (racks may be partial or full)
-
Close the instrument door and touch the Next button to start the automated preprocessing of samples.
Maxprep™ Liquid Handler Preprocessing Protocol
The Maxprep™ Liquid Handler will prepare samples prior to extraction using the Maxwell® RSC or Maxwell® RSC 48 Instruments. The following steps are performed by the Maxprep™ Liquid Handler:
- The system prepares a lysis reaction consisting of the following components:
- white blood cell lysate in 14ml tube
- 25µl of Proteinase K Solution
- 200µl of Lysis Buffer
- The Lysate incubates for 10 minutes.
- During the lysis incubation, plungers are transferred to each of the cartridges in the Maxwell® RSC or Maxwell® RSC 48 deck tray(s). The specified volume of Nuclease-Free Water is transferred to the elution tubes for each position in the Maxwell® RSC or Maxwell® RSC 48 deck tray(s), and 10µl of DNase I Solution is transferred to well# 4 of each of the cartridges in the Maxwell® RSC or Maxwell® RSC 48 deck tray(s).
- After lysis incubation is complete, each sample is transferred from the 14ml tube to its corresponding Maxwell® RSC cartridge.
- Method is complete. Open the instrument door and move the deck tray(s) to the Maxwell® RSC or Maxwell® RSC 48 Instrument for extraction. Remove primary sample tubes, processing plate, and used tips from the waste bin, and discard as hazardous waste following your institution’s recommended guidelines. Either discard or tightly cap and store remaining reagents.
Consumables for Maxprep™ preprocessing methods are designed to be used with potentially infectious substances. Use appropriate protective equipment (e.g., gloves and goggles) when handling infectious substances. Adhere to your institutional guidelines for the handling and disposal of all infectious substances when used with this system.
Maxwell® Instrument Setup and Run
Refer to the Maxwell® RSC Instrument Operating Manual #TM411 or Maxwell® RSC 48 Instrument Operating Manual #TM510 for more detailed information.
-
Turn on the Maxwell® instrument and Tablet PC. Sign in to the Tablet PC and start the Maxwell® software by double-touching the icon on the desktop. The instrument will power up, proceed through a self test and home all moving parts.
-
Touch Start to access the extraction ‘Methods’ screen. When running in Portal mode, scan the bar code(s) on the deck tray(s). After data has been returned from the Portal database, touch Continue to use the sample tracking information for the deck tray(s) or touch New to start a run and enter new sample tracking information.
-
On the ‘Methods’ screen, if a method has not been selected by scanning the bar code on the deck tray(s), select a method using one of the two options below:
-
Touch the simple RNA Blood method.
-
Use a bar code reader to scan the 2D bar code on the kit box to automatically select the appropriate method.
-
Verify that the simply RNA Blood method has been selected, and touch the Proceed button. If requested by the software, enter any kit lot and expiration information that has been required by the Administrator.
-
On the ‘Cartridge Setup’ screen (if shown), touch the cartridge positions to select or deselect any positions to be used for this extraction run. Enter any required sample tracking information, and touch the Proceed button to continue.
Note: When using the Maxwell® RSC 48, use the Front and Back buttons to select and deselect cartridge positions on each deck tray. -
Maxwell® Instrument Setup and Run (continued)
After the door has been opened, confirm that all Extraction Checklist items have been performed. Verify that samples were added to well #1 of the cartridges, cartridges are loaded on the instrument, uncapped elution tubes are present with Nuclease-Free Water and plungers are in well #8. Transfer the deck tray(s) containing the prepared cartridges onto the Maxwell® Instrument platform.
Inserting the Maxwell® deck tray(s): Hold the deck tray by the sides to avoid dislodging cartridges from the deck tray. Ensure that the deck tray is placed in the Maxwell® Instrument with the elution tubes closest to the door. Angle the back of the deck tray downward and place into the instrument so that the back of the deck tray is against the back of the instrument platform. Press down on the front of the deck tray to firmly seat the deck tray on the instrument platform. If you have difficulty fitting the deck tray on the platform, check that the deck tray is in the correct orientation. Ensure the deck tray is level on the instrument platform and fully seated.
Note: When using the Maxwell® RSC 48 Instrument, check the identifier on the Maxwell® RSC 48 deck tray to determine whether it should be placed in the front or back of the instrument. -
Touch the Start button to begin the extraction run. The platform will retract, and the door will close.
Note: When using the Maxwell® RSC 48 Instrument, if the Vision System has been enabled, the deck trays will be scanned as the door retracts. Any errors in deck tray setup (e.g., plungers not in well #8, elution tubes not present and open) will cause the software to return to the ‘Cartridge Setup’ screen and problem positions will be marked with an exclamation point in a red circle. Touch the exclamation point for a description of the error and resolve all error states. Touch the Start button again to repeat deck tray scanning and begin the extraction run. Warning: Pinch point hazard.
The Maxwell® Instrument will immediately begin the purification run. The screen will display information including the user who started the run, the current method step being performed and the approximate time remaining in the run.
Notes:- Touching the Abort button will abandon the run. All samples from an aborted run will be lost.
- If a run is abandoned before completion, you may be prompted to check whether plungers are still loaded on the plunger bar. If plungers are present on the plunger bar, perform Clean Up when requested.
If plungers are not present on the plunger bar, you can choose to skip Clean Up. The samples will be lost.
-
Follow the on-screen instructions at the end of the method to open the door. Verify that the plungers are located in well #8 of the cartridge at the end of the run. If the plungers are not removed from the plunger bar, follow the instructions in the Maxwell® RSC Instrument Operating Manual or the Maxwell® RSC 48 Instrument Operating Manual to perform a Clean Up process to unload the plungers.
-
Remove the deck tray(s) from the instrument. Remove elution tubes containing RNA, and cap the tubes. After the run has been completed, the extraction run report will be displayed. From the ‘Report View’ screen, you can print or export this report or both.
-
Remove the cartridges and plungers from the deck tray(s), and discard as hazardous waste following your institution’s recommended guidelines. Do not reuse reagent cartridges, plungers or elution tubes. Ensure samples are removed before performing any required UV light treatment to avoid damage to the nucleic acid.
Storing Eluted RNA
If sample eluates are not processed immediately, the eluted RNA should be
stored at –20°C or –70°C for up to
24 hours in the Maxwell® Elution Tubes. If longer term storage is desired,
transfer the eluted RNA into RNase-free labware that is suitable for long-term
storage and store at –70°C or below. Consult the instructions for downstream
applications for specific sample storage and handling recommendations.
Troubleshooting
For questions not addressed here, please contact your local Promega Branch Office or Distributor. Contact information available at: www.promega.com. E-mail: techserv@promega.com
Symptoms Low RNA yield, RNA degradation or poor reproducibility between samples
Causes and Comments
- The sample contains a low amount of RNA. The amount of RNA present in a sample depends on the metabolic state and white blood cell count.
- The blood sample was too old. Best yields are obtained with fresh blood. Samples that have been stored at 2–10°C for more than 3 days may give reduced yields. Stability of individual messages may vary.
- Use fresh blood; do not freeze the blood. For best results, do not freeze the cell pellet. However, the cell pellet resuspended in 1-Thioglycerol/Homogenization Solution mixture may be frozen.
- The wrong method was run with the Maxwell® Instrument.
- Lysis Buffer was added to whole blood instead of Cell Lysis Solution. Both red and white blood cells are lysed by Lysis Buffer, so there would be little or no pellet.
- 1-Thioglycerol was not added to the Homogenization Solution.
- Lysis Buffer was not added or was added in the wrong order.
- Lysates were not mixed sufficiently. Lysates must be mixed by vortexing for 20 seconds.
Appendix
9.A. Creating a Ribonuclease-Free Environment
Ribonucleases (RNases) are extremely difficult to inactivate. Take care to
avoid introducing RNase activity into your RNA samples during and after
isolation. This is especially important if the starting material was difficult
to obtain or is irreplaceable. The following notes may help prevent accidental
RNase contamination of your samples.
-
Two of the most common sources of RNase contamination are the user’s hands and bacteria or molds that may be present on airborne dust particles. To prevent contamination from these sources, use sterile technique when handling the reagents supplied with this system. Wear gloves at all times. Change gloves whenever ribonucleases may have been contacted.
-
Whenever possible, sterile, disposable plasticware should be used for handling RNA. These materials generally are RNase-free and do not require pretreatment to inactivate RNase.
-
Treat nonsterile glassware, plasticware and electrophoresis chambers before use to ensure that they are RNase-free. Bake glassware at 200°C overnight, and thoroughly rinse plasticware with 0.1N NaOH, 1mM EDTA, followed by RNase-free water. Commercially available RNase removal products also may be used, following the manufacturer’s instructions.
Note: Electrophoresis chambers may be contaminated with ribonucleases, particularly RNase A, from analysis of DNA samples. Whenever possible, set aside a new or decontaminated apparatus for RNA analysis only. -
Treat solutions not supplied with the system by adding diethyl pyrocarbonate (DEPC) to 0.1% in a fume hood. Incubate overnight with stirring at room temperature in the hood. Autoclave for 30 minutes to remove any trace of DEPC.
Caution: DEPC is a suspected carcinogen and should only be used in a chemical fume hood. DEPC reacts rapidly with amines and cannot be used to treat Tris buffers.
! Note: For all downstream applications, it is essential that you continue to protect your RNA samples from RNases. Continue to wear clean gloves and use solutions and centrifuge tubes that are RNase-free.
Related Products Instrument and Accessories
9.B. Related Products
Instrument and Accessories Product
|
Size
|
Cat.#
---|---|---
Maxwell® RSC Instrument| 1 each| AS4500
Maxwell® RSC 48 Instrument| 1 each| AS8500
Maxwell® RSC Plunger Pack| 1 each| AS1670
Maxwell® RSC/CSC Deck Tray| 1 each| SP6019
Maxwell® RSC/CSC 48 Front Deck Tray| 1 each| AS8401
Maxwell® RSC/CSC 48 Back Deck Tray| 1 each| AS8402
Maxprep™ Carrier, Maxwell® RSC| 1 each| AS9402
Maxprep™ Carrier, Maxwell® RSC 48 Front| 1 each| AS9403
Maxprep™ Carrier, Maxwell® RSC 48 Back| 1 each| AS9404
Maxprep™ Liquid Handler, RSC Carriers| 1 each| AS9100
Maxprep™ Liquid Handler, RSC Carriers w/ UV light| 1 each| AS9101
Maxprep™ Liquid Handler, RSC 48 Carriers| 1 each| AS9200
Maxprep™ Liquid Handler, RSC 48 Carriers w/ UV light| 1 each| AS9201
2.0ml Deep Well Plates (Non-Sterile)| 60/pack| AS9309
2.0ml Deep Well Plates (Sterile)| 60/pack| AS9307
Maxprep™ 1000µl Conductive Disposable Tips, Filtered| 40/box| AS9303
Maxprep™ 300µl Conductive Disposable Tips, Filtered| 60/box| AS9302
Maxprep™ Reagent Reservoir, 50ml| 28/pack| AS9304
Maxprep™ Waste Bags, Clear| 100/Box| AS9305
Maxprep™ Plunger Holder| 1 each| AS9408
Maxprep™ 3-Position Reagent Tube Holder| 1 each| AS9409
ClickFit Microtube, 1.5ml| 1,000/pack| V4741
Maxwell ® **RSC Reagent Kits**
For a list of available Maxwell® RSC purification kits, visit: www.promega.com.
| |
Summary of Changes
The following changes were made to the 4/22 revision of this document:
- Updated Sections 7 and 9.B.
- Edited text in Section 3.A.
- Incorporated other general text updates.
U.S. Pat. No. 6,855,499, European Pat. Nos. 1368629, 2090655 and 2363476,
Japanese Pat. No. 4399164 and other patents.
© 2014–2022 Promega Corporation. All Rights Reserved.
Maxwell is a registered trademark of Promega Corporation. Maxprep is a
trademark of Promega Corporation.
Nunc is a trademark of Nalge Nunc International. Products may be covered by
pending or issued patents or may have certain limitations. Please visit our
Web site for more information.
All prices and specifications are subject to change without prior notice.
Product claims are subject to change. Please contact Promega Technical
Services or access the Promega online catalog for the most up-to-date
information on Promega products. Promega Corporation · 2800 Woods Hollow Road
· Madison, WI 53711-5399 USA · Toll Free in USA
800-356-9526 ·
608-274-4330 · Fax
608-277-2516 15
www.promega.com TM417 · Revised 4/22
References
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