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Glycogen (DNase, RNase free)

€ 118,00

This product is molecular biology grade, free of DNase and RNase, and can be used as a carrier to increase the recovery of nucleic acids from diluted solutions by alcohol precipitation.

Package: 500μl

Description

This product is molecular biology grade, free of DNase and RNase, and can be used as a carrier to increase the recovery of nucleic acids from diluted solutions by alcohol precipitation.

As a precipitant for nucleic acids, glycogen works better than tRNA or sonicated DNA in most cases. Since glycogen does not contain DNA and RNA, the nucleic acids precipitated with glycogen is more suitable for subsequent PCR, RT-PCR, and  endonuclease reactions.

It was reported that precipitation of ligation products with glycogen has no interference with subsequent bacterial transformations.  Glycogen of 0.001mg/ml will not inhibit TdT, glycogen of no more than 2mg/ml will not affect the activity of reverse transcriptase, and 0.02mg/ml glycogen will not inhibit T4 RNA ligase. However, glycogen interferes with DNA-protein interactions.

Usually, 1μl of Glycogen (20mg/ml) can precipitate at least picogram (pg) of DNA or RNA from 1ml of solution. Each package of this product is sufficient to precipitate 500 DNA or RNA samples in conventional quantities.

Packing List:
Cat. No. Product Name Pack Size
D0812 Glycogen (20mg/ml) 500μl
– Information Sheet 1 copy

 

Storage Conditions:

Store at -20℃, valid for at least 1 year.

Precautions:

Usually, 1μl of Glycogen (20mg/ml) is sufficient for each sample. If glycogen may interfere with subsequent reactions, the amount of glycogen can be appropriately reduced, or tRNA can be used as a precipitant instead.

This product is for R&D only. Not for drug, household, or other uses.

For your safety and health, please wear a lab coat and disposable gloves during the operation.

Additional information

Weight 1 kg
Dimensions 30 × 30 × 20 cm

Instruction

Instructions for Use:

1. Add 1μl of Glycogen (20mg/ml) to DNA or RNA solutions and mix well.
Note: For specific experiments, the amount of glycogen can be adjusted appropriately.
2. Add ethanol or other precipitants to precipitate DNA or RNA.
Note: After adding precipitant and mixing, place the mixture at -20ºC or -80ºC for several hours or overnight to precipitate DNA or RNA thoroughly.
3. Centrifuge at 12,000×g for 10 minutes to obtain DNA or RNA pellet containing glycogen.

Product files

MSDS

https://scandicbiotech.com/wp-content/uploads/2026/04/D0812-1018.pdf

References

Related papers:

1. CHENG P, LI RS, LIN BY, WANG WQ, LI YH, GUO Y, LI W.
.
Reprod Contracept. 2009 Mar; 20(1):1-9. (IF 0.33)
2. Yao X, Ei-Samahy MA, Feng X, Zhang T, Li F, Zhang G, Pang J, Nie H, Wang F.
.
Anim Reprod Sci. 2017 Dec;187:159-166. (IF 1.66)
3. Dongdong Qin, Yayun Gu, Yu Zhang, Shu Wang, Tao Jiang, Yao Wang, Cheng Wang, Chang Chen, Tao Zhang, Weiya Xu, Hanben Wang, Ke Zhang, Liangjun Hu, Lufan Li, Wei Xie, Xin Wu, Zhibin Hu
.
Nat Commun. 2023 Dec 11;14(1):8209. doi: 10.1038/s41467-023-43480-z.
4. Hongyun Wang, Jiangpeng Feng, Cong Zeng, Jiejie Liu, Zhiying Fu, Dehe Wang, Yafen Wang, Lu Zhang, Jiali Li, Ao Jiang, Miao He, Yuanyuan Cao, Kun Yan, Hao Tang, Deyin Guo, Ke Xu, Xiang Zhou, Li Zhou, Ke Lan, Yu Zhou, Yu Chen
.
Emerg Microbes Infect. 2023 Dec;12(1):2178238. doi: 10.1080/22221751.2023.2178238.

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