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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 保质期：
3年
- 英文名：
Glucomannan Assay Kit
- 库存：
1
- 供应商：
上海经科化学科技有限公司
- 保存条件：
常温/冷藏
- 规格：
50 Assays
葡甘露聚糖检测试剂盒介绍：
| Content: | 50 assays per kit |
| Shipping Temperature: | Ambient |
| Storage Temperature: | Short term stability: 2-8oC, Long term stability: See individual component labels |
| Stability: | > 2 years under recommended storage conditions |
| Analyte: | Glucomannan |
| Assay Format: | Spectrophotometer |
| Detection Method: | Absorbance |
| Wavelength (nm): | 340 |
| Signal Response: | Increase |
| Linear Range: | 4 to 80 μg of glucomannan per assay |
| Limit of Detection: | 1 g/100 g |
| Total Assay Time: | 120 min |
| Application examples: | Jelly sweets, cosmetics, food gums and other materials. |
| Method recognition: | Novel method |
- Very cost effective
- Only enzymatic kit available
- Simple format
- All reagents stable for > 2 years after preparation
- Mega-Calc™ software tool is available from our website for hassle-free raw data processing
- Standard included
The Glucomannan test kit is suitable for the measurement and analysis of Glucomannan in plant products and food.
View more of our polysaccharide test kits.
葡甘聚糖检测试剂盒说明书(PDF)请向客服索取！
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文献和实验McCleary, B. V., Charnock, S. J., Rossiter, P. C., O’Shea, M. F., Power, A. M. & Lloyd, R. M. (2006). Journal of the Science of Food and Agriculture, 86(11), 1648-1661.
McCleary, B. V., Gibson, T. S. & Mugford, D. C. (1997). Journal of AOAC International, 80, 571-579.
microliters of 0.5M EDTA, 20 microliters 1M Tris-HCl, pH 6.5 and 2 microliters of 10mg/ml Proteinase K to the combined eluates and incubate for one hour at 45�C. 14, Recover DNA by phenol/chloroform extraction and ethanol precipitation. Addition
Chromatin IP (CHIP assay) This protocol has some minor modification to the protocol described in Strahl-Bolsinger S. et al. [1997, Gen & Dev 11, p83-93] and was obtained from Flick K. (The Scripps Research Institute).
Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
the amplification criteria used in the original 3C assay, subsequent to the reversal of cross-linking and purification (Dekker et al. 2002). View larger version (18K): [in this window] [in a new window]
