脂質(zhì)體2000/Lip2000

產(chǎn)品簡(jiǎn)介
脂質(zhì)體2000轉(zhuǎn)染試劑轉(zhuǎn)染試劑是一種多用途轉(zhuǎn)染試劑，可在各種貼壁和懸浮細(xì)胞系中提供高效轉(zhuǎn)染。研究人員可使用 Lipofectamine 2000試劑進(jìn)行基于 siRNA和 shRNA的基因敲除實(shí)驗(yàn)及基因表達(dá)研究。 Lipofectamine 2000是索萊寶公司提供的用于 siRNA和質(zhì)粒 DNA共轉(zhuǎn)染的最佳試劑。脂質(zhì)體2000/Lip2000

產(chǎn)品型號(hào)：L7800

更新時(shí)間：2025-08-07

廠商性質(zhì)：生產(chǎn)廠家

訪問(wèn)量：2217

產(chǎn)品咨詢 18101056239

產(chǎn)品分類

技術(shù)文章

細(xì)胞凋亡染色試劑盒可以檢測(cè)細(xì)胞內(nèi)凋亡信號(hào)

如何配置常用染色液

關(guān)于PCR，你知道多少？（四） ----幾種特殊的PCR

了解甘油三酯(TG)含量檢測(cè)原理

詳細(xì)介紹在線留言

Lip2000 is a newly developedand proprietary reagent for the transfection of nucleic acids into eukaryoticcells.

Lip2000 has the followingadvantages:

The highest transfectionefficiency in many cell types and formats.

DNA-Lip2000 complexes can bedirectly added to cells in culture medium (with or without serum).

It is not necessary to removeDNA-Lip2000 complexes or change medium following transfection.

The complexes can be removedafter 4-6 hours by replacing with refresh medium (optional)

Contents andStorage

Lip2000 is supplied in liquidform at a concentration of 1mg/ml. Store at 4℃.DONOT FREEZE.

ProductQualification

Lip2000 has been extensivelytested by transfection of HEK293 cells with an EGFP reporter containing

plasmid. Lip2000 is free ofmicrobial contamination.

ImportantGuidelines

Follow these guidelines whenperforming transfections:

1. The ratio of DNA (in μg) :Lip2000 (in μl) to use when preparing complexes should be 1:2 to 1:3 for mostcell lines. To transfect 0.5 -2 ×10⁵cells in a24-well format, use 0.8-1 μg DNA and 2-3 μl of Lip2000. Optimizingtransfection by varying DNA/Lip2000 ratio is possible.

2. It isCRITICALtotransfect cells at high cell density. 90-95% confluence the time oftransfection is recommended to obtain high efficiency and expression levels andto minimize decreased cell growth associated with high transfection activity.Lower cell densities are suitable with optimization of conditions. Take care tomaintain a standard seeding protocol between experiments because transfectionefficiency is dependent on culture confluence.

3.DO NOTaddantibiotics to media during transfection as this will cause cell death.

For better results, you maychoose to:

Use Opti-MEM I medium to diluteLip2000 prior to complexing with DNA. Other media without serum (e.g.DMEM) maybe used to dilute Lip2000,but transfection efficiency maybe compromised.

Note:Some serum-free formulationscan inhibit Lip2000 mediated transfection, for example:CD 293, 293 SFM II, and VP-SFM etc.

TransfectionProcedure for 24-Well Format

For adherent cells:One day before transfection,plate cells in growth medium (withoutantibiotics) so that they will be 90-95% confluent at the time of transfection(0.5 -2 ×10⁵cells/well for a24-well plate).

For suspension cells: On the day of transfectionjust prior to preparing complexes,plate 4-8×10⁵cells/500 μl of growth medium(without antibiotics) in a 24-well plate.

1. For each transfection sample, prepare DNA-Lip2000 complexes as follows:

? Dilute DNA in 50 μl ofOpti-MEM I Reduced Serum Medium without serum (or other medium without serum).Mix gently.

? Mix Lip2000 gently beforeuse, then dilute the appropriate amount in 50 μlofOpti-MEMI Medium (or other medium without serum). Mix gently and incubatefor 5 minutes at room temperature.

Note: Combine the dilutedLip2000 with the diluted DNA within 30 minutes. Longer incubation times maydecrease activity. If DMEM is used as a diluent for the Lip2000, mix with thediluted DNA within 5 minutes. After the 5 minute incubation,combine the diluted DNA with the dilutedLip2000 (total volume is100 μl).

?Mix gently and incubate for 20 minutes at roomtemperature to allow the DNALip2000 complexes to form. The solution may appearcloudy,but this will not inhibit the transfection.

Note:DNA-Lip2000 complexes are stable forat least 5 hours at room temperature.

2. Add the 100 μl of DNA-Lip2000 complexesto each well. Mix gently by rocking the plate back and forth.

3. Incubate the cells at 37℃ in a CO2 incubator for 24-48 hours until they are readyto assay for transgene expression. It is not necessary to remove the complexesor change the medium;however,growth medium may be replaced after 4-6hours without loss of transfection activity.

For stable cell lines:Passage the cells at a 1:10 or higherdilution into fresh growth medium 24 hours after transfection. Add selective mediumthe following day.

For suspension cells:Add PMA and/or PHA (if desired) 4 hoursafter adding the DNA-Lip2000 complexes to the cells.

Tip: For Jurkat cells, adding PHA-L and PMA at final concentrations of 1 μg/ml and 50 ng/ml, respectively, enhances CMV promoter activity and gene expression. ForK562 cells, adding PMA alone is sufficient to enhance promoteractivity.

Scaling Up orDown Transfections

To transfect cells in differenttissue culture formats, vary the amounts of Lip2000 , DNA, cells, and medium used in proportionto the difference in surface area (see table below). With automated, highthroughput systems, larger complexing volumes are recommendedfor transfections in 96-well plates. Note: You may perform rapid 96-well platetransfections (plate cells and transfect simultaneously) by adding a suspensionof cells directly to complexes prepared in the plate. Prepare complexes and addcells at twice the cell density as