Features:
1. Brushless frequency motor with simpler construction, more reliable performance, longer life and quietly running
2. Automatically electric lid lock, super speed, over temperature protection and imbalance protection. The centrifuge body is made of high quality steel, safe and reliable.
3. Rotor is connected to spindle by specialized taper sleeve, loading simple and quick, no direction, safe and reliable.
4. Microprocessor control.
5. Digital display in time, speed and RCF.
6. 10 kinds of program stored in the memory, 10 kinds of accelerating and decelerating speed for your choice.
7. 3 tiers protection steel cover, stainless steel chamber, safe and reliable.
TG20Technical Parameter:
Max. Speed | 21000rpm |
Max. RCF | 30910×g |
Max. Capacity | 6×100ml |
Time Range | 0~99min |
RPM/RCF Convert | Yes |
Noise (dB) | ≤60 |
Temperature | Normal |
Acc/Dec | 10 Kinds |
Speed Accuracy | ±20r/min |
Temperature Accuracy | / |
Voltage(V/Hz) | AC 220V/110V 50HZ/60HZ |
Size (W x D x Hmm) | 513×370×320mm |
Net Weight/Gross weight(Kg) | 43KG/60KG |
Certificates | CE,ISO & Calibration report are available |
Matched Rotors for TG20
Order no | Rotor | Max Speed(r/min) | Volume(ml) | Max RCF(*g) |
G20-1 | Fixed Rotor | 16000 | 4×8PCR | 15760 |
G20-2 | Fixed Rotor | 15000 | 6×8PCR | 21420 |
G20-3 | Fixed Rotor | 16000 | 8×8PCR | 17480 |
G20-4 | Fixed Rotor | 15000 | 12×8PCR | 22930 |
G20-5 | Fixed Rotor | 21000 | 12×1.5/2ml | 30910 |
G20-6 | Fixed Rotor | 15000 | 40×0.5ml | 22920 |
G20-7 | Fixed Rotor | 17000 | 24×1.5/2ml | 26460 |
G20-8 | Fixed Rotor | 13500 | 30×1.5/2ml | 19340 |
G20-9 | Fixed Rotor | 13000 | 48×1.5/2ml | 17930 |
G20-10 | Fixed Rotor | 16000 | 16×5ml | 22020 |
G20-11 | Fixed Rotor | 16000 | 6×10ml | 21500 |
G20-12 | Fixed Rotor | 15000 | 12×10ml | 22680 |
G20-13 | Fixed Rotor | 16000 | 12×7ml | 21380 |
G20-14 | Fixed Rotor | 13000 | 16×10ml | 19490 |
G20-15 | Fixed Rotor | 11000 | 12×15ml | 14330 |
G20-16 | Fixed Rotor | 13000 | 8×15ml(conical) | 17790 |
G20-17 | Fixed Rotor | 5000 | 24×15ml | 3500 |
G20-18 | Fixed Rotor | 15000 | 8×20ml | 22680 |
G20-19 | Fixed Rotor | 5000 | 30×15ml | 3830 |
G20-20 | Fixed Rotor | 14000 | 6×30ml | 19060 |
G20-21 | Fixed Rotor | 13000 | 6×50ml(conical) | 18840 |
G20-22 | Fixed Rotor | 13000 | 6×50ml(round) | 18730 |
G20-23 | Fixed Rotor | 13000 | 4×85ml | 18940 |
G20-24 | Fixed Rotor | 12000 | 6×70ml | 15570 |
G20-25 | Fixed Rotor | 12000 | 4×100ml | 14850 |
G20-26 | Fixed Rotor | 10000 | 6×100ml | 11380 |
G20-27 | Fixed Rotor | 18000 | 30×0.5ml | 26660 |
G20-28 | Swing Rotor | 13000 | 4×5ml | 14960 |
G20-29 | Vertical Rotor | 16000 | 16×5ml | 16540 |
G20-30 | Vertical Rotor | 14000 | 8×30ml | 16450 |
G20-31 | Microplate Rotor | 4000 | 2×3×48(well) | 2300 |
Norgen’s Plant/Fungi Total RNA Purification Kit provides a rapid method for the isolation and purification of total RNA, including virus and viroid RNA, from a wide range of plants. Total RNA can be purified from fresh or frozen plant tissues, plant cells or filamentous fungi samples using this kit. All sizes of RNA are purified, including microRNA (miRNA) . The procedure is rapid and convenient.
The RNA is purified without the use of phenol or chloroform. The purified RNA is of the highest quality, and can be used in a number of downstream applications including real time PCR, reverse transcription PCR, Northern blotting, RNase protection and primer extension, and expression array assays.
Norgen’s Plant/Fungi Total RNA Purification Kit is also available in a 96-well (High Throughput) format for high throughput applications. Purification with the 96-well plates can be performed using either a vacuum manifold or centrifugation.
Figure 1 / 4
Click for expanded view
Kit Specifications – Spin Column | |
Maximum Column Binding Capacity | 50 μg |
Maximum Column Loading Volume | 650 μL |
Size of RNA Purified | All sizes, including small RNA (< 200 nt) |
Maximum Amount of Starting Material: Plant Tissues Plant Cells Fungi | 50 mg 1 x 106 cells 50 mg (wet weight) |
Average Yield* 50 mg Tomato Leaves 50 mg Tobacco Leaves 50 mg Plum Leaves 50 mg Grape Leaves 50 mg Peach Leaves | 60 μg 60 μg 32 μg 35 μg 30 μg |
Time to Complete 10 Purifications | 30 minutes |
* Yield will vary depending on the type of sample processed.
* Yield will vary depending on the type of sample processed.
Storage Conditions and Product Stability
All solutions should be kept tightly sealed and stored at room temperature. This kit is stable for 2 years after the date of shipment.
Tobacco (Nicotiana tabacum)
Tomato (Lycopersicon esculentum)
Pepper (Capsicum annuum)
Potato (Solanum tuberosum)
Arabidopsis thaliana1
Peach (Prunus persica)
Apple (Malus sp.)
Pear (Pyrus sp.)
Grape vine (Vitis sp.)
Plum (Prunus sp.)
Palm (Arecaceae)
Pine needle (Pinaceae)
Strawberry
Raspberry
Blackberry
Herbs
Persimmon (Ebenaceae)
Potato tuber (Solanum)
Plum fruit
Citrus
Vanilla bean
Cotton (Gossypium)
Mangrove
Chrysanthemum
Grape berry skin
Kiwi leaves
Peach (fruits and flowers)
Soy bean (legume)
Eastern White Red Cedar
Corn leaves
Cucumber leaves
Aspergillus niger
Mucor racemosus
Cladosporium cladosporioides
Fusarium oxysporum
Penicillium sp.
Botrytis cinerea (Botryotinia fuckeliana)
Pichia sp.
Rhizopus oryzae
Alternaria tenuissima
Component | Cat. 25800 (50 preps) | Cat. 31350 (100 preps) | Cat. 25850 (250 preps) | Cat. 31900 (192 preps) |
---|---|---|---|---|
Lysis Buffer C | 60 mL | 1 x 30 mL, 1 x 60 mL | 3 x 60 mL | 2 x 60 mL |
Wash Solution A | 38 mL | 38 mL | 1 x 18 mL, 2 x 38 mL | 2 x 38 mL |
Elution Solution A | 6 mL | 6 mL | 20 mL | 20 mL |
Filter Columns | 50 | 100 | 250 | – |
Spin Columns | 50 | 100 | 250 | – |
96-Well Plate | – | – | – | 2 |
Adhesive Tape | – | – | – | 4 |
Collection Tubes | 100 | 200 | 500 | – |
96-Well Collection Plate | – | – | – | 2 |
Elution Tubes (1.7 mL) | 50 | 100 | 250 | – |
96-Well Elution Plate | – | – | – | 2 |
Product Insert | 1 | 1 | 1 | 1 |
The NGS FFPE DNA Library Prep Kit (illumina and MGI Platforms) was developed for the construction of high quality FFPE DNA libraries using 10 ng to 400 ng of input DNA isolated from formalin-fixed, paraffin-embedded (FFPE) samples. The DNA damage caused by fixation makes it difficult to construct high quality libraries. Our kit has been optimized to repair damaged DNA in the reactions. Multiplexing of the NGS FFPE DNA Library is possible.
FFPE samples are a great resource for biomedical research. However, the methods for fixation and condition of storage significantly damage the DNA in the samples. Thus, the extraction of high quality DNA from FFPE samples is often a challenge. Low yield and low quality of FFPE DNA usually are common because of the limited tissue material and the DNA degradation.
As a result, it is usually difficult to construct high quality NGS libraries from low amount and low quality of FFPE DNA. In order to address this issue, we have developed the NGS FFPE DNA Library Prep Kit to make high quality libraries from the low input of FFPE DNA samples.
Three index types are available for the NGS FFPE DNA Library Prep Kit of the illumina platform:
Non-index (Cat.# 30035): Libraries do not have index.
Index (Cat.# 30037): Each of our index primers contains a unique barcode DNA (6 bases long) that can be used to identify individual library. Multiplexing of libraries is up to 48 samples. Index information can be downloaded here.
Unique dual index (Cat.# 30039): FFPE DNA library multiplexing is possible with 96 samples based on the unique dual indexing system. Our unique Four–Base Difference Index System allows us to make indexes that have at least 4 bases different from each other in the 8-base index sequence. Our unique dual indexing primers can effectively remove NGS errors including index hopping, de-multiplexing errors, index cross-contamination, mis-assignments etc. The unique dual index primer set includes 96 pre-mixed unique pairs of i5 and i7 index primers. Index information can be downloaded here.
Indexes are available for the MGI platform kits (Cat.# 34037).
Kit advantages:
The NGS FFPE DNA Library Prep Kit (illumina and MGI Platforms) was developed for the construction of high quality FFPE DNA libraries using 10 ng to 400 ng of input DNA isolated from formalin-fixed, paraffin-embedded (FFPE) samples. The DNA damage caused by fixation makes it difficult to construct high quality libraries. Our kit has been optimized to repair damaged DNA in the reactions. Multiplexing of the NGS FFPE DNA Library is possible.
83, On-nut 88/2 Prawet Sub-district, Prawet District, Bangkok, 10250, Thailand
Tel : 081-875-1869 , 02-328-7179
Email : [email protected]
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