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Boston Biochem/Tunicamycin/3516/10

价格
¥3560.00
货号:3516/10
浏览量:103
品牌:Boston Biochem
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商品描述
Product Details
Citations (8)
Reviews (3)
Biological Activity Technical DataBackground Product DatasheetsCalculators

Biological Activity

Antibiotic; inhibits GlcNAc phosphotransferase (GPT). Blocks the formation of N-glycosidic linkages by inhibiting the first step in glycoprotein synthesis. Activity induces ER stress and causes G1 arrest; can be used to induce autophagy. Tunicamycin contains four main components as follows:
  • Homolog A, n=8, C37H60N4O16, molecular weight = 816.90
  • Homolog B, n=9, C38H62N4O16, molecular weight = 830.93
  • Homolog C, n=10, C39H64N4O16, molecular weight = 844.95
  • Homolog D, n=11, C40H66N4O16, molecular weight = 858.99
The composition of this product will vary from batch to batch and can be found on the relevant certificate of analysis.

Technical Data

M.Wt:
844.95
Formula:
C39H64N4O16 (tunicamycin C, n=10)
Solubility:
Soluble to 50 mM in DMSO
Storage:
Store at +4°C
CAS No:
11089-65-9

The technical data provided above is for guidance only.For batch specific data refer to the Certificate of Analysis.Tocris products are intended for laboratory research use only, unless stated otherwise.

Background References

  1. The hepatitis B virus precore protein is retrotransported from endoplasmic reticulum (ER) to cytosol through the ER-associated pathway.Duriez et al.J.Biol.Chem., 2008;283:32352
  2. Primary murine airway smooth muscle cells exposed to poly(I:C) or tunicamycin synthesize a leukocyte-adhesive hyaluronan matrix.Lauer et al.J.Biol.Chem., 2009;284:5299
  3. Differential effects of endoplasmic reticulum stress-induced autophagy on cell survival.Ding et al.J.Biol.Chem., 2007;282:4702

Product Datasheets

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Citations for Tunicamycin

The citations listed below are publications that use Tocris products.Selected citations for Tunicamycin include:

8Citations: Showing 1 - 8

  1. Caspase-mediated cleavage of IRE1 controls apoptotic cell commitment during endoplasmic reticulum stress.Authors: Shemorry Et al.Elife2019;8
  2. A CASPR1-ATP1B3 protein interaction modulates plasma membrane localization of Na+/K+-ATPase in brain microvascular endothelial cells.Authors: Zhang Et al.J Biol Chem2019;
  3. ONC201 kills breast cancer cells in vitro by targeting mitochondria.Authors: Greer Et al.Oncotarget2018;9:18454
  4. Hyperactivation of nuclear receptor coactivators induces PERK-dependent cell death.Authors: Hossain Et al.Oncotarget2018;9:11707
  5. N-Glycosylation Regulates the Trafficking and Surface Mobility of GluN3A-Containing NMDA Receptors.Authors: Skrenkova Et al.Front Mol Neurosci2018;11:188
  6. Tumor-Suppressor Inactivation of GDF11 Occurs by Precursor Sequestration in Triple-Negative Breast Cancer.Authors: Bajikar Et al.Dev Cell2017;43:418
  7. NCOA3 coactivator is a transcriptional target of XBP1 and regulates PERK-eIF2α-ATF4 signalling in breast cancer.Authors: Gupta Et al.Oncogene2016;35:5860
  8. ER stress induces anabolic resistance in muscle cells through PKB-induced blockade of mTORC1.Authors: Deldicque Et al.PLoS One2011;6:e20993

FAQs

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Reviews for Tunicamycin

Average Rating: 4.7(Based on 3 Reviews)

5 Star
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Usage Information
By Anonymouson 06/20/2020
Application: Species:Human

5 μg/ml

PMID: 31453810Reference

Worked at once
By Bibha Dahalon 01/08/2020
Application: Species:Human

I dissolved tunicamycin in DMSO. I added tunicamycin at various concentrations (2uM, 4uM, 6uM, and 10uM) for 24 hours in human primary astrocytes and incubated at 37 C and 5% CO2. Next day, I collected lystates and ran a western blot. The first four lanes are tunicamycin added samples in increasing concentration and the last two lanes are without added. I looked for PERK activation using p-PERK antibody.


Tunicamycin Usage Information
By Chao Lion 01/08/2018
Application: Species:Human

It is working well and easily dissolved into DMSO. I used 2.5, 5 µg/ml of Tunicamycin with serum free culture medium to treat the cells for 8h, 16h, 24h, and 48h.


Boston Biochem波士顿生物化学已与IQ Proteomics™合作,为分析您的泛素化蛋白提供定制服务。使用哈佛医学院Gygi实验室开发的泛素绝对定量(AQUA)技术,我们可以对样品中存在的不同泛素连接进行定量表征。