The HiPure Total RNA Kit provides fast purification of high-quality RNA from cells, tissues, and yeast using silica-membrane spin columns with a binding capacity of 100μg RNA. There is no need for phenol/chloroform extractions and time-consuming steps such as CsCl gradient ultracentrifugation or isopropanol precipitation. RNA purified using the HiPure Total RNA Purification System can be used for applications such as RT-PCR, Northern blotting, poly A+ RNA (mRNA) purification, nuclease protection, and in vitro translation.
Specifications
Features | Specifications |
Main Functions | Isolation total RNA (not include miRNA) from animal tissues, cells and simple plant tissues using one column |
Applications | RT-PCR, qRT-PCR, Northern hybridization, second generation sequencing |
Purification method | Mini spin column |
Purification technology | Silica technology |
Process method | Manual (centrifugation or vacuum) |
Sample type | Animal soft tissue, cultured cells, lymphocytes, simple plant tissue |
Sample amount | Cells: ≤1 x 107 Animal tissue: 1-20 mgPlant leaves: 50-150 mg Yeast cells: 5 x 106 |
Yield | 2-100μg |
Elution volume | ≥50μl |
Time per run | ≤15 minutes(1-24 samples) |
Liquid carrying volume per column | 800µl |
Binding yield of column | 100µg |
HiPure RNA technology simplifies total RNA isolation. Samples are first lysed and then homogenized. Ethanol is added to the lysate to provide ideal binding conditions. The lysate is then loaded onto the HiPure silica membrane and RNA binds to the silica membrane, and all contaminants are efficiently washed away. For certain RNA applications that are sensitive to very small amounts of DNA, the residual amounts of DNA remaining can be removed using a convenient on-column DNase treatment. Pure, concentrated RNA is eluted in water.
Advantages
Kit Contents
Contents | R401102 | R401103 |
Purification Times | 50 Preps | 250 Preps |
HiPure RNA Mini Columns | 50 | 250 |
2ml Collection Tubes | 50 | 250 |
RTL Lysis Buffer | 50 ml | 200 ml |
RNA Binding Buffer | 15 ml | 75 ml |
Buffer RW1 | 50 ml | 200 ml |
Buffer RW2* | 20 ml | 2 x 50 ml |
RNase Free Water | 10 ml | 30 ml |
Storage and Stability
The Kit can be stored dry at room temperature (15-25°C) and are stable for at least 18 months under these conditions.
The HiPure Total RNA Kit provides fast purification of high-quality RNA from cells, tissues, and yeast using silica-membrane spin columns with a binding capacity of 100μg RNA. There is no need for phenol/chloroform extractions and time-consuming steps such as CsCl gradient ultracentrifugation or isopropanol precipitation. RNA purified using the HiPure Total RNA Purification System can be used for applications such as RT-PCR, Northern blotting, poly A+ RNA (mRNA) purification, nuclease protection, and in vitro translation.
Product Details
Sensitivity:
High
Kit Type:
RNA
Format:
Lyophilized
Reaction Volume:
50 μL
Reagents:
Enzymes, Buffers, And Primers
Product Name:
Overall Solution For Thermostatic Detection Of Largemouth Bass Rhabdovirus
Storage Temperature:
-20°C
High Light:
,
,
Payment & Shipping Terms
Minimum Order Quantity
48T
Price
USD3.8$/T
Packaging Details
16T/Bag,48T/Box
Delivery Time
6days
Payment Terms
T/T paypal
Supply Ability
100000T/Month
Reagent component ( WLB8201KIT ,16T/bags,48T/Box ) | |||
Component | Specification | Quantity | Function |
E buffer | 1ml | 2Tube | Buffer systems primarily used for protein/enzyme stabilization and performance |
B buffer | 0.15ml | 1Tube | Mainly activated systems such as magnesium ions |
Positive control template | 0.1ml | 1Tube | Mainly the positive plasmid template is used to test the effectiveness of the kit |
Reagent Guide Manua | 16T/bags,48T/Box | 3 bags | Reagent technology of protein/enzyme system: freeze-dried powder, freeze-dried microspheres |
This kit is based on a rapid nucleic acid amplification technology at room temperature and constant temperature: at room temperature and constant temperature (generally 39ºC~42ºC), with the help of auxiliary proteins and single-strand binding proteins,the recombinase and primers form a complex; Source search and combine the target homology domain, at this time, a D-loop region is formed at the homology position and strand exchange begins;along with the dissociation of the recombinase from the complex,the polymerase also binds to the 3′ end of the primer and begins chain extension.It is suitable for laboratory-level DNA amplification and DNA amplification for other detection purposes.
Intended Usage:
For cultivating fastidious bacteria.
Principle:
Tryptone, peptone, and yeast extract multivalent powder provides a nitrogen source, vitamins, and growth factors; sodium chloride to maintain osmotic balance; glucose carbon source; dipotassium hydrogen phosphate as a buffering agent.
Formulation(per liter):
Tryptose 20.0g
Glucose 2.0g
Dipotassium hydrogen phosphate 2.5g
Sodium chloride 5.0g
Final pH 7.3±0.2
How to use:
Suspend 29.5g in 1L of purified water. Heat with frequent agitation to dissolve the powder.
Sterilize at 121℃ for 15 minutes
Storage:
Keep the container tightly closed. Store in a cool, dry place, away from bright light. The storage period is 3 years.
Specification: 500g/bottle
500g
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Tel : 081-875-1869 , 02-328-7179
Email : hej@a3p-scientific.com
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