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Cell Biolabs彗星實(shí)驗(yàn)試劑盒

由于環(huán)境因素和細(xì)胞內(nèi)的正常代謝過程造成的DNA損傷,每個(gè)細(xì)胞每天都會發(fā)生1,000到1,000,000個(gè)。雖然這些只占人類基因組約60億個(gè)堿基中的一小部分,但如果關(guān)鍵基因損傷未及時(shí)修復(fù),可能會阻礙細(xì)胞的正常生理功能,進(jìn)而增加癌變可能。彗星實(shí)驗(yàn),或稱單細(xì)胞凝膠電泳(Single cell gel electrophoresis,SCGE是一種測量單個(gè)細(xì)胞DNA損傷的常用技術(shù)。其原理簡單,即在電泳場,將受損細(xì)胞DNA(包含片段和鏈斷裂)與完整的DNA分離,通過顯微鏡觀察到損傷細(xì)胞呈現(xiàn)出典型的彗星狀尾巴,然后通過測量計(jì)算彗尾大小對比出細(xì)胞DNA損傷的程度。因?yàn)?/span>彗星實(shí)驗(yàn)特點(diǎn),該方法幾乎被用來評估任何類型的真核細(xì)胞的 DNA 修復(fù)能力,包括雙、單鏈斷裂的不同的 DNA 損傷情況。是一種能快速、大通量檢測真核細(xì)胞DNA損傷進(jìn)而判別遺傳毒性的技術(shù)。

彗星實(shí)驗(yàn)結(jié)果圖

彗星實(shí)驗(yàn)原理簡單,但操作繁瑣,需要豐富的實(shí)驗(yàn)經(jīng)驗(yàn)和技巧,尤其常常出現(xiàn)的“脫膠”問題,困擾了科研人員除此之外,有時(shí)為了跑出完美的“彗星”圖案放在paper里,還需要重復(fù)做許多次實(shí)驗(yàn),費(fèi)時(shí)費(fèi)力。為了解決上述問題,我們推薦CellBiolabsOxiSelectTMComet Assay Kit即彗星實(shí)驗(yàn)試劑盒來檢測細(xì)胞的DNA損傷。該試劑盒不僅能讓彗星實(shí)驗(yàn)化繁為簡,還兩種不同規(guī)格(3孔和96孔)的細(xì)胞電泳凝膠板供選擇,讓少量樣本和大量樣本的DNA損傷檢測通通輕松hold住。用該試劑做彗星實(shí)驗(yàn)流程如下圖。

除了操作簡便,OxiSelectTMComet Assay Kit還有以下優(yōu)點(diǎn):

1)      適用于各種DNA損傷檢測,是一款非常好用的DNA損傷檢測篩選工具;

2)      試劑盒中的載玻片經(jīng)過特殊處理以粘附低熔點(diǎn)瓊脂糖,避免“脫膠”問題出現(xiàn);

3)      采用特殊的DNA熒光染料,能有效降低背景干擾,更加方便讀取實(shí)驗(yàn)結(jié)果。


彗星實(shí)驗(yàn)試劑盒信息:

品名

貨號

規(guī)格

說明

OxiSelectTM Comet Assay Kit (3-Well Slides)

STA-350

15 assays

試劑盒內(nèi)有53孔載玻片和彗星實(shí)驗(yàn)所需的低熔點(diǎn)瓊脂糖、裂解液及DNA熒光染料,共可檢測15個(gè)樣品。

OxiSelectTM Comet Assay Kit (3-Well Slides)

STA-351

75 assays

試劑盒內(nèi)有25張3孔載玻片和彗星實(shí)驗(yàn)所需的低熔點(diǎn)瓊脂糖、裂解液及DNA熒光染料,共可檢測75個(gè)樣品。

OxiSelectTM Comet Assay Kit (96-Well Slides)

STA-355

96 assays

試劑盒內(nèi)有1張96孔載玻片和彗星實(shí)驗(yàn)所需的低熔點(diǎn)瓊脂糖、裂解液及DNA熒光染料,共可檢測96個(gè)樣品。



為了
滿足客戶更多樣的實(shí)驗(yàn)需求,彗星實(shí)驗(yàn)試劑盒內(nèi)特殊處理電泳載玻片可以單獨(dú)購買,詳情如下:

 


品名

貨號

規(guī)格

產(chǎn)品圖片

Comet Assay Slides, 3-Well

STA-352

5 slides

STA-353

25 slides

Comet Assay Slides, 96-Well

STA-356

1 slides

STA-356-5

5 slides

產(chǎn)品部分發(fā)表文獻(xiàn):


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  15. Siemionow, M. et al. (2020). Transplantation of Dystrophin Expressing Chimeric (DEC) Human Cells of Myoblast/MSC Origin Improves Function in Duchenne Muscular Dystrophy Model. Stem Cells Dev. doi: 10.1089/scd.2020.0161.
  16. Lammert, C.R. et al. (2020). AIM2 inflammasome surveillance of DNA damage shapes neurodevelopment. Nature. doi: 10.1038/s41586-020-2174-3.
  17. Shibayama, Y. et al. (2020). Aberrant (pro)renin receptor expression induces genomic instability in pancreatic ductal adenocarcinoma through upregulation of SMARCA5/SNF2H. Commun Biol. 3(1):724. doi: 10.1038/s42003-020-01434-x.
  18. Han, J. et al. (2020). Elevated CXorf67 Expression in PFA Ependymomas Suppresses DNA Repair and Sensitizes to PARP Inhibitors. Cancer Cell. doi: 10.1016/j.ccell.2020.10.009.
  19. Hays, E. et al. (2020). The SWI/SNF ATPase BRG1 stimulates DNA end resection and homologous recombination by reducing nucleosome density at DNA double strand breaks and by promoting the recruitment of the CtIP nuclease. Cell Cycle. doi: 10.1080/15384101.2020.1831256.
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