Features
1.Maintenance -free brushless motor
2.LCD display of Speed, RCF and time.
3.Adjustable speed from 300r/min to 5000r/min
4.Timer from 1s to 99min or continuous operation
5.For 6x15ml centrifuge tube &10ml/7ml/5ml/3ml blood collection tube or 4x50ml centrifuge tube
6.Lid automatically open at the end of run to revent sample warming and to reduce handling time.
7.10 Program stored in memory and editable by ender user.
8.10 Acceleration/ 10 Deceleration profiles ,with soft brake system to get the good separation effect.
9.Electric cover lock, compact design, super speed and imbalance protection.
The D-Glucosamine test kit is a high purity reagent for the measurement and analysis of D-glucosamine in neutraceutical/food products. This kit can also be used to measure N-Acetyl-D-Glucosamine and D-Glucosamine sulphate.
Note for Content: The number of manual tests per kit can be doubled if all volumes are halved. This can be readily accommodated using the MegaQuantTM Wave Spectrophotometer (D-MQWAVE).
All reagents stable for > 2 years after preparation
All enzymes supplied as stable suspensions
Very rapid reaction
Mega-Calc™ software tool is available from our website for hassle-free raw data processing
Standard included
Suitable for manual, microplate and auto-analyser formats
Document
The D-Glucosamine test kit is a high purity reagent for the measurement and analysis of D-glucosamine in neutraceutical/food products. This kit can also be used to measure N-Acetyl-D-Glucosamine and D-Glucosamine sulphate.
Format Lyophilized In Vitro Diagnostic Test Kits With High Sensitivity
Product Info
Document
Product Info
Product Description
Format Lyophilized In Vitro Diagnostic With High Sensitivity
Product Detail
Kit Storage and term of Validity
Storage term: stored at ≤-20℃,keep away from light, avoid heavy weight and repeated freezing and thawing.
Term of Validity: 14 months
Isothermal nucleic acid Principle Summary
This kit is based on a rapid nucleic acid amplification technology at room temperature and constant temperature:at room temperature and constant temperature(generally 39℃~42℃),reverse transcriptaseuses specific primers and template RNA tosynthesize cDNA strands,and binds the auxiliary protein and single strand with the help of the protein, the recombinase and the primer form a complex; perform a homology search and bind the target homology domain, at this time a D-loop region is formed at the homology positionand strand exchange begins; accompanied by the recombinase from the complex upon dissociation,the polymerase also bindsto the 3′ end of the primer,initiating chainextension.It is suitable for laboratory-level RNA amplification and RNA amplification for other detection purposes.
Isothermal nucleic acid Product Features
1/ High sensitivity and specificity, short reaction time.
2/ The reagent form is freeze-dried, stable and easy to operate.
3/ The reaction can be operated by metal bath and water bath pot without purchasing expensive PCR apparatus.
Technical Parameters:
Parameters
Details
Product Name
RNA Isothermal Amplification Kit Basic
Manufacturer
Amp-future
Storage Temperature
-20°C
Kit Components
Enzymes, Buffers ,Reagents
Packaging
48 Tests/box
Detection Limit
500-1000copies/µL
Shipping
ICE
Test Time
5-20mins
Isothermal nucleic acid Applications
Suitable for RNA isothermal rapid amplification kit(BASIC type)
Primer: Require pair of nucleotide primers with the length of 25-35 bp.
RNA basic kit reaction temperature is 39 to 42℃ and time is 5-20 minutes.
Notes
1/ Please avoid nucleic acid contamination and set blank control during reaction due to the high sensitivity of the kit.
2/ Please take out the required quantity of MIRA reaction units for the experiment, and put the rest under storage conditions when performing the experiment.
The PCR Decontamination Kit can remove contaminating DNA in PCR master mixes, without reduction of PCR sensitivity.
The double-strand specific property of the dsDNase allows decontamination with primers and probe present.
Efficient for end-point PCR, probe-based qPCR, and some SYBR based qPCR mixes.
Contaminating bacterial DNA can be reduced to levels below the detection limit.
Fast and easy protocol.
Flat NTCs (No Template Controls).
Decontamination of master mixes without reduction of sensitivity has always been a challenge. Especially when minor amounts of DNA are targeted, contaminating DNA is a major problem. Any loss of sensitivity in the qPCR assay caused by the decontamination protocol is unacceptable.
In Figure 1, it is demonstrated that the PCR decontamination kit can remove contaminating DNA from a qPCR mix to non-detectable levels (flat NTC), without affecting the sensitivity of the qPCR.
Kit Contents
DTT (Inactivation Aid)
dsDNase
Document
The PCR Decontamination Kit can remove contaminating DNA in PCR master mixes, without reduction of PCR sensitivity.