
Description
Specifications
Clone | IHC969 |
Source | Mouse Monoclonal |
Positive Control | Thyroid Gland |
Dilution Range | 1:200 |
Tau proteins are abundant in neurons of the central nervous system, and function in microtubule stability and organization. Defects in Tau functioning and aggregation of these proteins have been clinically linked to a number of neurodegenerative disorders including Alzheimer’s disease, Parkinson’s disease, Pick’s disease (PiD), progressive supranuclear palsy (PSP), cortical basal degeneration (CBD), and frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17).
Clone | IHC969 |
Source | Mouse Monoclonal |
Positive Control | Thyroid Gland |
Dilution Range | 1:200 |
DBCO-PEG2-acid is an analog of DBCO-Acid with PEG linker and a DBCO group. The DBCO groups is commonly used for copper-free Click Chemistry reactions due to its strain promoted high energy. The hydrophilic PEG chain allows for increased water solubility. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
DBCO-PEG2-acid is an analog of DBCO-Acid with PEG linker and a DBCO group. The DBCO groups is commonly used for copper-free Click Chemistry reactions due to its strain promoted high energy. The hydrophilic PEG chain allows for increased water solubility. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
Magnetic bead nucleic acid purification technology uses nano or micron superparamagnetic material as the matrix, generally black ferric oxide or yellowish brown ferricoxide as the magnetic material. The surface of bead is coated with appropriate functional groups, which can adsorb nucleic acid. Magnetic beads commonly used for nucleic acids, containing carboxyl groups, hydroxyl groups, or silicon groups. Silicon-based magnetic beads are the most common, and its principle of adsorbing nucleic acid is consistent with the classical glass milk purification technology or glass fiber filter membrane purification method. Magpure particle is a kind of polydisperse fast speed silica magnetic beads. The core is ferricoxide, accounting for 50%, and the surface coating is silica, accounting for 50%. The product can be used for plasmid extraction, gel DNA recovery, product purification, genomic DNA and RNA extraction, and viral nucleic acid extraction.
Specifications
Features | Specifications |
Concentration | 10 mg/ml |
Appearance | Suspension of yellowish brown particles |
Surface functional group | Carboxyl, COOH |
Dispersibility | Monodisperse, spherical |
Particle size | 0.8-1 μm |
Preservation conditions | Room temperature, valid for up to 2 years.It is recommended to store in 2-8°C to prevent microbial growth. |
Magnetic response speed | 120 seconds |
Settling velocity | >2 hours |
High salt mediated binding | No adsorption |
Alcohol mediated binding | 1M NaClO4/ethanol(50%), DNA/RNA recovery up to 90% |
PEG8000 mediated binding | The recovery of DNA/RNA was up to 90% |
DNase/RNase | Not detected |
DNA residue | Not detected |
Recommended application | Plasmid extraction, gel DNA recovery, genomic DNA extraction and RNA extraction. |
Principle
Highsalt mediated binding: in the solution containing 2-4M guanidine isothiocyanate, Magpure particles can selectively recover DNA molecules, and impurities such as protein polysaccharides are not adsorbed.
Alcohol mediated binding: in the solution containing guanidine salt and alcohol (>25%), Magpure particles can selectively recover DNA/RNA molecules, and proteins and other impurities are not adsorbed.
After biological samples are treated with digestive solution or lysis Buffer, DNA/RNA is released from cells, organelles and protein complexes (ribosomes and nucleosomes) into reagents. After Magpure particles and binding solution are added, DNA/RNA is adsorbed to the surface of Magpure particles to form DNA/RNA bead complex. Under the action of the magnetic field, the magnetic beads are separated and collected, and the impurities such as protein are removed with the waste liquid. After two or three steps of further cleaning, the DNA/RNA magnetic bead complex is resuspended in sterilized water or TE buffer, and the DNA/RNA falls off from the surface of the magnetic beads, so as to achieve the purpose of purification.
Ordering information
CAT.No. | Product Name | Package |
C14130 | MagBind Particles | 10 ml |
C14131 | MagBind Particles | 100 ml |
Features | MagPure Particles | MagPure Particles N | MagPure Particles G | MagPure Particles F | MagBind Particles |
Cat.No. | C1410 | C1411 | C1412 | C1414 | C1413 |
Concentration | 100mg/ml | 70mg/ml | 40mg/ml | 50mg/ml | 10mg/ml |
Form | Amorphous and Porous | Amorphous and Porous | Porous | Amorphous | Nonporous |
Surface function | Si-OH, Silica Beads | Si-OH, Silica Beads | Si-OH, Silica Beads | Si-OH, Silica Beads | COOH, Carboxyl Beads |
Dispersion | Polydisperse | Polydisperse | Monodisperse | Monodisperse | Monodisperse |
Particle Size | 1.5-5μm | 0.2-2μm | 1-1.5μm | 0.2-1.5μm | 0.8-1μm |
Color | Black | Yellowish Brown | Dark Brown | Dark Brown | Yellowish Brown |
Magnetic response | 15-30s | ~60s | ~30s | 20s | 120s |
Settling Time (1ml) | >5min | >10min | >3min | >3min | >2h |
Usage (0.2ml Sample) | 20μl | 20μl | 20-30μl | 20-30μl | 20-30μl |
DNA Recover Rate (only 4M GITC) | >80% | >80% | >80% | >80% | 0 |
DNA Recover Rate (10% PEG8000/NaCl) | >85% | >85% | >85% | >85% | >90% |
Recommended Use | gDNA/RNA Isolation from Blood, Tissue, Plant, Swab, Spots, Stool, Soil and etc.Viral DNA/RNA IsolationAgarose Gel DNA Purification | DNA/RNA Isolation from low nucleic acid content samplesPlasmid IsolationDNA/RNA Clean Up | Circulating DNA IsolationViral Nucleic acid IsolationgDNA Isolation FFPE DNA/RNA Isolation | Plasmid extractiongel DNA recoverygenomicDNA/RNA extraction viral nucleic acid extractionCirculating DNA extraction | DNA/RNA Clean Up and concentrationDNA/RNA Isolation from low nucleic acid content samplesResearch immuno assays |
Magnetic bead nucleic acid purification technology uses nano or micron superparamagnetic material as the matrix, generally black ferric oxide or yellowish brown ferricoxide as the magnetic material. The surface of bead is coated with appropriate functional groups, which can adsorb nucleic acid. Magnetic beads commonly used for nucleic acids, containing carboxyl groups, hydroxyl groups, or silicon groups. Silicon-based magnetic beads are the most common, and its principle of adsorbing nucleic acid is consistent with the classical glass milk purification technology or glass fiber filter membrane purification method. Magpure particle is a kind of polydisperse fast speed silica magnetic beads. The core is ferricoxide, accounting for 50%, and the surface coating is silica, accounting for 50%. The product can be used for plasmid extraction, gel DNA recovery, product purification, genomic DNA and RNA extraction, and viral nucleic acid extraction.
Features
1.Brushless frequency motor, in great torque, free maintenance, no powder pollution, quick in speed up and down.
2.Imported compressors fluorine free,double cycle cooling, cold and hot alternating easily, free environment pollution and precise in temperature control.
3.Microprocessor control, digital display which indicates the temperature, speed, time, RCF in operation, speed raising and reducing quickly, operate simply. Running parameter can be edited.
4. 10 kinds of program stored in the memory, 10 kinds of accelerating and decelerating speed for your choice.
5. Automatically electric lid lock, over speed, over temperature protection and imbalance protection.
6.High quality steel centrifuge body , stainless steel chamber, built-in stainless steel explosion-proof protect sleeve , 3 tiers protection,safe and reliable.
7. Rotor is connected to spindle by specialized spring taper sleeve, loading simple and quick, no direction
8. With pre-cooling and get the ideal centrifugation result.
TGL16 Technical Parameter:
Max. Speed | 16000rpm |
Max. RCF | 20600×g |
Max. Capacity | 6×100ml |
Time Range | 1~9h59min |
RPM/RCF Convert | Yes |
Noise (dB) | ≤ 58 |
Acc/Dec | 10 Kinds |
Speed Accuracy | ±20r/min |
Temperature Accuracy | ±1℃ |
Voltage(V/Hz) | AC 220V/110V 50HZ/60HZ |
Size (L x W x Hmm) | 610×570×370mm |
Net Weight(Kg) | 82KG |
Certificates | TUV CE,ISO 9001,ISO13485 & Calibration report are available |
Matched Rotor for TGL16
Order No | Rotor | Max speed (rpm) | Max Volume(ml) | Max RCF (g) |
G16-1 | Angle rotor | 14000 | 4×8PCR | 12070 |
G16-2 | Angle rotor | 13000 | 6×8PCR | 16080 |
G16-3 | Angle rotor | 14000 | 8×8PCR | 13390 |
G16-4 | Angle rotor | 13000 | 12×8PCR | 17220 |
G16-5 | Angle Rotor | 15000 | 30×0.5ml | 18510 |
G16-6 | Angle Rotor | 14000 | 40×0.5ml | 19970 |
G16-7 | Angle Rotor | 16000 | 12×1.5/2ml | 17940 |
G16-8 | Angle Rotor | 15000 | 24×1.5/2ml | 20600 |
G16-9 | Angle Rotor | 13500 | 30×1.5/2ml | 19340 |
G16-10 | Angle Rotor | 11000 | 48×1.5/2ml | 12840 |
G16-11 | Angle Rotor | 15000 | 16×5ml | 19350 |
G16-12 | Angle Rotor | 14000 | 12×7ml | 16370 |
G16-13 | Angle Rotor | 14000 | 6×10ml | 16460 |
G16-14 | Angle Rotor | 12000 | 12×10ml | 14510 |
G16-15 | Angle Rotor | 10000 | 12×15ml | 11840 |
G16-16 | Angle Rotor | 5000 | 24×15ml | 3080 |
G16-17 | Angle Rotor | 5000 | 30×15ml | 3830 |
G16-18 | Angle Rotor | 12000 | 8×20ml | 14510 |
G16-19 | Angle Rotor | 12000 | 6×30ml | 14000 |
G16-20 | Angle Rotor | 11000 | 6×50ml | 13480 |
G16-21 | Angle Rotor | 12000 | 6×70ml | 10810 |
G16-22 | Angle Rotor | 8000 | 6×100ml | 7280 |
G16-23 | Angle Rotor | 12000 | 24 pieces capillary vessel | 15800 |
G16-24 | Microplate rotor | 4000 | 2×3×48 Well | 2300 |
83, On-nut 88/2 Prawet Sub-district, Prawet District, Bangkok, 10250, Thailand
Tel : 081-875-1869 , 02-328-7179
Email : hej@a3p-scientific.com
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