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当前位置: 首页 > 产品中心 > Spectrophotometer > 生物测定系统/PiBlue™磷酸盐分析试剂盒/500试验/POPB-500
商品详细生物测定系统/PiBlue™磷酸盐分析试剂盒/500试验/POPB-500
生物测定系统/PiBlue™磷酸盐分析试剂盒/500试验/POPB-500
生物测定系统/PiBlue™磷酸盐分析试剂盒/500试验/POPB-500
商品编号: POPB-500
品牌: bioassaysys
市场价: ¥4180.00
美元价: 2090.00
产地: 美国(厂家直采)
公司:
产品分类: 分光光度计
公司分类: Spectrophotometer
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

PiBlue™ Phosphate Assay Kit

PiBlue™ Phosphate Assay Kit Catalog No: POPB-500
Price: $209 Qty:
For orders of 10 or more kits, please call +1-510-782-9988x1 oremail us for best pricing and/or bulk order. Shipping: RT Shipment: Fedex ServiceDelivery: 1-2 days (US), 3-6 days (Intl) Storage: 4°C
Phosphate Assay Kit (POPB-500)
  • Product Overview
  • Product FAQ
  • Product Citations
  • Assay Service
ProtocolSDS

Application

  • For sensitive and high-throughput phosphate determination.

Key Features

  • Reagent very stable. Due to our innovative formulation, no precipitation of reagent occurs. Therefore no filtration of reagent is needed prior to assays, as is often required with other commercial kits.
  • High sensitivity and wide detection range: detection of as little of 20 pmoles of phosphate and useful range between 0.4 μM and 50 μM phosphate.
  • Fast and convenient: single reagent "mix-and-measure" assay allows quantitation of free phosphate within 30 minutes.
  • Compatible with routine laboratory and HTS formats: assays can be performed in tubes, cuvettes or microplates, on spectrophotometers and plate readers.
  • Robust and amenable to HTS: Z factors of 0.7 to 0.9 are observed in 96-well plates. Can be readily automated on HTS liquid handling systems

Method

  • OD620nm (malachite green)

Samples

  • Enzyme reactions with free phosphate releases

Species

  • All

Size

  • 500 tests

Detection Limit

  • 0.4 μM

Shelf Life

  • 12 months

More Details

  • The PiBlue™ Phosphate Assay Kit is based on a proprietary formulation of the malachite green dye. The PiBlue™ reagent forms a blue colored complex with free orthophosphate. The rapid color formation from the reaction can be conveniently measured on a spectrophotometer (600 - 660 nm) or on a plate reader. The non-radioactive colorimetric assay kits have been optimized to offer superior sensitivity and prolonged shelf life. The assay is simple and fast, involving a single addition step for phosphate determination. Assays can be performed in tubes, cuvettes or multi-well plates. The assays can be conveniently executed in 96-well plates for high-throughput screening of enzyme inhibitors.

What is the difference between your 3 phosphate assays: DIPI-500, POMG-25H, POPB-500?

All three products are based on the malachite green dye. While the PiBlue (POPB-500) and QuantiChrom (DIPI-500) Phosphate Assay Reagents are identical, they differ in the standards. The PiBlue is designed for customers who want prepare a full calibration curve for their assays, and the latter has one set of a blank control and 30 µM phosphate standard. The reagent is more diluted than the reagent used in the Malachite Green Phosphate Assay Kit (POMG-25H). As a result, one adds 100 µL reagent (POPB-500 or DIPI-500) to 50 µL sample, whereas for the Malachite Green based assay, one adds 20 µL Reagent to 80 µL sample. In practice, the DIPI-500 is the most convenient kit to use, because there is no need to prepare a calibration curve there is no need for extra mixing. Because adding a larger volume (100 μL) to a small volume (50 μL) effects efficient mixing in well, no extra mixing is needed. The POPB-500 requires preparation of calibration curve. With the POMG-25H Kit, one needs to mix the reagent with the sample, because adding 20 µL to 80 µL does not mix efficiently by itself. Also a preparation of a standard curve is necessary.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.
Hwang, J. D., Ortiz-Maldonado, M., & Paramonov, S. (2016). Delivery of Formulated Industrial Enzymes with Acoustic Technology. Journal of laboratory automation, 21(1), 153-165. Assay: Phosphate in Buttiauxella sp Phytase. Demidenko AA et al (2011). Effects of viscogens on RNA transcription inside reovirus particles. J Biol Chem. 286(34):29521-30. Assay: Phosphate in rat lipid.Liu Q et al (2011). Competition between foliar Neotyphodium lolii endophytes and mycorrhizal Glomus spp. fungi in Lolium perenne depends on resource supply and host carbohydrate content. Functional Ecology 25:910-920. Assay: Phosphate in mouse intracellular phosphate.Lopez-Vales R, et al (2010). Fenretinide promotes functional recovery and tissue protection after spinal cord contusion injury in mice. J Neurosci. 30(9):3220-6. Assay: Phosphate in mouse lipid. Oborna I et al (2010). Increased lipid peroxidation and abnormal fatty acid profiles in seminal and blood plasma of normozoospermic males from infertile couples. Hum Reprod. 25(2):308-16. Assay: Phosphate in fish marine teleost follicles, eggs. Oborna I et al. (2010). Increased lipid peroxidation and abnormal fatty acid profiles in seminal and blood plasma of normozoospermic males from infertile couples. Hum Reprod. 25(2):308-16. Assay: Phosphate in human blood, semen. Polewski MD, et al (2010). Inorganic pyrophosphatase induces type I collagen in osteoblasts. Bone 46(1):81-90. Assay: Phosphate in mouse/human cellular extract. Cramp RL et al (2009). Ups and downs of intestinal function with prolonged fasting during aestivation in the burrowing frog, Cyclorana alboguttata. J Exp Biol. 212(22):3656-63. Assay: Phosphate in mouse lipid.Cramp RL, et al (2009). Ups and downs of intestinal function with prolonged fasting during aestivation in the burrowing frog, Cyclorana alboguttata. J Exp Biol. 212(22):3656-63. Assay: Phosphate in frog Na+/K+-ATPase extract. Huxtable AG, et al (2009). Tripartite purinergic modulation of central respiratory networks during perinatal development: the influence of ATP, ectonucleotidases, and ATP metabolites. JNeurosci. 29(47):14713-25. Assay: Phosphate in rat ATPase extract. Kang HY et al (2008). Altered TNSALP expression and phosphate regulation contribute to reduced mineralization in mice lacking androgen receptor. Mol Cell Biol.28(24):7354-67. Assay: Phosphate in rat ATPase extract.Kang HY, et al (2008). Altered TNSALP expression and phosphate regulation contribute to reduced mineralization in mice lacking androgen receptor. Mol Cell Biol.28(24):7354-67. Assay: Phosphate in mouse cytosolic fraction. Chen X et al (2007). The isolation and structure of membrane lipid rafts from rat brain. Biochimie 89(2):192-6. Assay: Phosphate in mouse/human cellular extract.Chen X, et al (2007). The isolation and structure of membrane lipid rafts from rat brain. Biochimie 89(2):192-6. Assay: Phosphate in rat lipid. Hough TA et al (2007). Novel mouse model of autosomal semidominant adult ypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2. J Bone Miner Res. 22(9):1397-407. Assay: Phosphate in frog Na+/K+-ATPase extract.Hough TA, et al (2007). Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2. J Bone Miner Res. 22(9):1397-407. Assay: Phosphate in mouse intracellular phosphate. Lau K.H. et al. (2006). An osteoclastic protein-tyrosine phosphatase is a potential positive regulator of the c-Src protein-tyrosine kinase activity: a mediator of osteoclast activity. J Cell Biochem. 97(5):940-55. Assay: Phosphate in rabbit phosphatases.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.
品牌介绍
BioAssay Systems位于加州北部,是一家专注于提供高质量试剂盒的生物技术公司,试剂盒种类广泛、使用简便、操作简单、快速且性能优越,用户不需花额外的时间来作调适测试。BioAssay Systems产品具有快速、简单、高通量(可用于HTS药物筛选)、灵敏(特别适合小鼠样品) 、准确性高和低干扰等主要特征,且采用发光、生物发光、化学发光、荧光等非放射性的检测技术,安全无害可靠。