BioAssay Systems/EnzyChrom™ Invertase Assay Kit/100 tests/EIVT-100

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货号:EIVT-100
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EnzyChrom™ Invertase Assay Kit

EnzyChrom™ Invertase Assay Kit Catalog No: EIVT-100
Price: $409 Qty:
For orders of 10 or more kits, please call +1-510-782-9988x1 oremail us for best pricing and/or bulk order. Shipping: On Ice Shipment: Fedex ServiceDelivery: 1-2 days (US), 3-6 days (Intl) Storage: 4, -20°C
Invertase/Sucrase Assay Kit
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ProtocolSDS

Application

  • For quantitative determination of invertase/sucrase activity.

Key Features

  • Safe. Non-radioactive assay.
  • Sensitive and accurate. As low as 0.007 U/L invertase activity can be quantified.
  • Homogeneous and convenient. "Mix-incubate-measure" type assay. No wash and reagent transfer steps are involved.
  • Robust and amenable to HTS: can be readily automated on HTS liquid handling systems for processing thousands of samples per day.

Method

  • OD570nm, or FL530/585nm

Samples

  • Biological, environment (soil) etc

Species

  • All

Size

  • 100 tests

Detection Limit

  • 0.007 U/L

Shelf Life

  • 6 months

More Details

  • Invertase(b-fructofuranosidase, EC 3.2.1.26) is an enzyme that catalyzes the hydrolysis of sucrose to fructose and glucose. Invertases cleave at the O-C(fructose) bond, whereas a related enzyme sucrase (EC 3.2.1.48) cleaves at the O-C(glucose) bond. A wide range of microorganisms produce invertase and can, thus, utilize sucrose as a nutrient. Invertase assay finds wide applications in environmental (e.g. soil), agricultural and food (confectionery) industry. BioAssay Systems Invertase Assay Kit provides a convenient and ultra-sensitive colorimetric and fluorimetric means to measure invertase activity. In the assay, invertase cleaves sucrose, resulting in the formation of fructose and glucose, which is determined by a colorimetric (570nm) or fluorimetric method (λex/em = 530/585nm). The assay is simple, sensitive, stable and high-throughput adaptable.

Can the EnzyChrom™ Invertase Assay be used to determine sucrase activity?

Yes, sucrase is the same as invertase.

How do I prepare honey samples?

Due to the high sugar content in honey, a 10 kDa cut-off centrifugal filter is needed in this experiment to remove background sugars (e.g. VWR Cat No: 82031-348). 1.) Accurately weigh out 10 mg of honey and dissolve it in 500 µL of H2O (50 fold dilution).2.) Add 500 µL of the dissolved honey into the centrifugal filter. Centrifuge at 12,000 × g at 4°C until most of the liquid (there should be less than 50 µL left) has passed through the membrane (~20 min). Dispose of the eluent.3.) To wash the invertase, add 500 µL of H2O to the tube and centrifuge at 12,000 × g at 4°C. Dispose eluent. Repeat wash one more time. Allow most of the liquid (less than 50 µL should remain) to pass through the filter.4.) Dilute the concentrated invertase in the filter membrane by adding 500 µL of 1X reaction buffer. The sample is ready to be assayed. Refer to the EIVT product datasheet for instructions.Note: Levels of invertase may vary in honey samples, therefore if the signal is to high, serially dilute the invertase sample to determine the appropriate dilution to work with and multiply the calculated activity by the dilution factor. If the signal is too low, adjust the dilution in step 4. Adjusted Calculation: Invertase Activity: ((Rsample - Rcontrol)/(slope × t)) × (5×10-4 L/10 mg) (U/mg) Where 5 ×10-4 L comes from the 500 µL of reaction buffer added to dilute the concentrated invertase in the membrane and 10 mg was the initial mass of honey.For more detailed product information and questions, please feel free to Contact Us. Or for more general information regarding our assays, please refer to our General Questions.
Chua, L. S., et al (2014). Effect of thermal treatment on the biochemical composition of tropical honey samples. International Food Research Journal 21(2): 773-778. Assay: Invertase in honey. Chua, L. S., et al.(2014). Effect of thermal treatment on the biochemical composition of tropical honey samples. International Food Research Journal 21(2): 773-778. Assay: Invertase/Sucrase in Honey.Ciesielska, K et al (2014). Exoproteome analysis of Starmerella bombicola results in the discovery of an esterase required for lactonization of sophorolipids. Journal of Proteomics(98):159-174. Assay: Invertase in S. bombicola protein extract.To find more recent publications, pleaseclick here.
If you or your labs do not have the equipment or scientists necessary to run this assay, BioAssay Systems can perform the service for you.Simply send us your samples:- Fast turnaround - Quality data - Low costPlease email or call 1-510-782-9988 x 2 to request assay service.
BioAssay Systems酸性磷酸酶(ACP)是一种在消化过程中催化磷酸基团从其他分子上裂解的酶。酸性磷酸酶可以在溶酶体中发现,并在与内体融合,酸化pH值后变得有活性,从而为ACP创造了最佳环境。ACP还可以在骨骼,脾脏,肝脏,肾脏和血液中发现。血清水平可以用作前列腺癌的生物标志物,尽管前列腺特异性抗原(PSA)被更广泛地使用。BioAssay Systems非放射性比色ACP分析基于从合成底物上裂解对硝基苯酚。加入终止剂后,对硝基苯酚会显色。加入终止剂后在405 nm处吸光度的增加与酶活性成正比。