Propargyl-PEG5-alcohol enables Click Chemistry reactions with azide compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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Propargyl-PEG5-alcohol enables Click Chemistry reactions with azide compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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TD4N Table Top 5000rpm Low Speed Laboratory Centrifuge
Product Info
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Product Info
TD4N Table Top 5000rpm Low Speed Laboratory Centrifuge
TD4N Features:
1. Microprocessor control, less noisily, it is widely used to qualitative analysis of blood serum, plasma and urea in the fields of hospital, blood center, laboratory and biochemistry.
2. Brushelss motor, free maintenance, no powder pollution, quick in speed up and down.
3. The flexible axle driven system which drive the rotor directly, smooth in operation and small vibration.
4. There are many rotors for your choice, suitable for different specifications meet customers’ different requirements of separation.
5. Micro-computer control system, digital display the RCF, time and speed.
6. Electric lid lock, compact design, super speed and imbalance protection.
TD4N Technical Parameter:
Max. Speed
5000rpm
Speed Accuracy
±20rpm
Max. Volume
6x100ml
Power Supply
AC110V/220V 50HZ/60HZ
Max. RCF
3460xg
Noise
≤55dBA
Timer
0~99min
Net Weight
18Kg
Dimension
540x370x280mm
Certifications
CE, ISO & Calibration report are available.
Warranty
1 Year
Matched Rotors for TD4N:
Order No.
Rotor Type
Max.Speed(rpm)
Max.Volume(ml)
Max.RCF(xg)
4N-1
Swing Rotor
5000
6x10ml
3460
4N-2
Angle Rotor
4000
30×7/5ml
2250
4N-3
Angle Rotor
4000
18×15/10ml
2250
4N-4
Angle Rotor
4000
24x10ml
2200
4N-5
Angle Rotor
4000
12×15/7/5ml
2150
4N-6
Angle Rotor
4000
12x20ml
2200
4N-7
Angle Rotor
5000
6x15ml
2540
4N-8
Angle Rotor
5000
12x15ml
3080
4N-9
Angle Rotor
5000
4x50ml
2520
4N-10
Angle Rotor
5000
6x50ml
2850
4N-11
Angle Rotor
5000
4x100ml
2630
4N-12
Angle Rotor
5000
6x100ml
3130
Document
TD4N is a table top centrifuge widely used to qualitative analysis of blood serum, plasma and urea in the fields of hospital, blood center, laboratory and biochemistry.
Opentrons 4-in-1 Tube Rack set includes 2 base stands and 4 tube holder tops: 1.5ml, 2ml, 15ml + 50ml, 15ml, and 50ml. The tube holder tops snap securely on the base stand, which fits directly on the deck. The Tube Rack Set is not autoclavable.
Document
Opentrons 4-in-1 Tube Rack set includes 2 base stands and 4 tube holder tops: 1.5ml, 2ml, 15ml + 50ml, 15ml, and 50ml. The tube holder tops snap securely on the base stand, which fits directly on the deck. The Tube Rack Set is not autoclavable.
Cat.# 20104S, 20104L: Size range 250-350 bp (ideal for NGS library size selection)
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The series of DNA Size Selection Kits (Magnetic Beads) were developed for DNA size selection using magnetic beads. A total of 11 kits are available, with different selection ranges spanning from 50 bp to over 10 kb. The kits provide a simple and quick approach for the enrichment of a specific range of DNA fragments. The kit workflow allows double-sided or single-sided size selection for specific size cutoffs.
Gel images of different ranges of size selection. Sheared human genomic DNA was used as input.
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DNA size selection is a selective capture of DNA fragments of a specific range of size for next-generation sequencing (NGS) library preparations, PCR, ChIP assay, DNA ligations, endonuclease digestions, adapter removal, and other genomics and molecular biology applications. DNA size selection is preferred after NGS library prep in most of the cases. The NGS library preparation is related to the quality of the sequencing data. Precise NGS library size selection can increase sequencing efficiency, improve data quality, and reduce costs.
There are two types of sequencing technologies: short-read sequencing and long-read sequencing. Short-read sequencing uses DNA libraries that contain small insert DNA fragments of similar sizes, usually several hundred base pairs. The sequencing efficiency can be improved if the DNA size selection is in the right range. Cat.# 20104S and 20104L are the best kits for NGS library size selection of illumina paired-end 100 (PE100) sequencing with 100-200 bp library inserts; Cat.# 20105S and 20105L are the best kits for NGS library size selection of illumina paired-end 150 (PE150) sequencing with 150-300 bp library inserts; and Cat.# 20106S and 20106L are the best kits for NGS library size selection of illumina paired-end 300 (PE300) sequencing with 300-600 bp library inserts.
Long-read sequencing uses a large DNA fragment as input and makes very long reads. Usually, library size selection is preferred to remove smaller fragments. Cat.# 20110S and 20110L are the best kits for long-read sequencing size selection with DNA sizes >5 kb, and Cat.# 20111S and 20111L are the best kits for long-read sequencing size selection with DNA sizes >10 kb.
The magnetic beads technology uses paramagnetic particles, also known as SPRI (Solid Phase Reversible Immobilization) beads, to bind DNA reversibly and selectively. DNA fragments can be size-selected and purified by changing the properties of the magnetic beads or SPRI beads. The magnetic beads can easily separate the beads-binding DNA from the contaminants and unwanted components in the samples. The samples after DNA size selection are free of contaminants such as buffer components, enzymes, proteins, salts, dNTPs, primers, and adapters. Our proprietary magnetic beads reagents improve yield, selectivity, and reproducibility.
Specific DNA fragments at a certain length range can be purified simply using magnetic separation with different beads components, avoiding tedious and time-consuming gel extraction and column-based purification. The magnetic beads method is popular for common DNA size selection, including library size selection. The first beads-binding step, referred to as the right-side clean-up, removes large DNA fragments. The large DNA fragments are bound to the beads and are discarded. The desired DNA fragments in the supernatant are transferred to a new well, and new beads are added to the supernatant for the second beads-binding, referred to as the left-side clean-up. The double-size selected DNA fragments are eluted after ethanol rinsing.
DNA size selection with dual clean-ups.
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A single clean-up is needed for DNA size selection with large fragments. In this case, only the large DNA fragments are bound to the beads. The selected larger DNA fragments are eluted after ethanol rinsing.
DNA size selection with single clean-up for >5 kb and >10 kb DNA.
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Features of DNA size selection and library size selection
High specificity and high recovery of size selection
11 selection ranges are available, including 5 ranges for NGS library size selection
50-100 bp
100-200 bp
200-500 bp
250-350 bp: ideal for illumina PE100 sequencing
300-450 bp: ideal for illumina PE150 sequencing
450-750 bp: ideal for illumina PE300 sequencing
500-1000 bp
1-3 kb
1-5 kb
>5 kb: ideal for long-read sequencing
>10 kb: ideal for long-read sequencing
Fast and simple
20-min protocol
No gel purification required
No columns required
No centrifugation required
Efficient removal of contaminants and unwanted components