Yes, Product PKH67 would be suitable for this application. In this paper, both Products PKH26 and PKH67 are used in a similar application:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5679712/
PKH67GL
PKH67 Green Fluorescent Cell Linker Kit for General Cell Membrane Labeling
Distributed for Phanos Technologies
동의어(들):
Green PKH membrane labeling kit
크기 선택
₩2,003,509
출고 가능일2025년 4월 16일세부사항
크기 선택
About This Item
₩2,003,509
출고 가능일2025년 4월 16일세부사항
추천 제품
Quality Level
포장
pkg of 1 kit
저장 조건
protect from light
형광
λex 490 nm; λem 502 nm (PKH67 dye)
검출 방법
fluorometric
배송 상태
ambient
저장 온도
room temp
애플리케이션
- To label and further investigate the exosomes expelled from cells in triple-negative breast cancer condition.[1]
- To label apoptotic cells,[2] in order to study the role of ανβ5 receptor in both binding and internalization of apoptotic cells.[3]
- In fluorescence imaging.[4]
Slow loss of fluorescence has been observed in in vivo studies using PKH1 and PKH2. PKH67 may exhibit similar properties since this behavior appears to be characteristic of green cell linker dyes, but not red cell linker dyes. Correlation of in vitro cell membrane retention with in vivo fluorescence half life in non-dividing cells predicts an in vivo fluorescence half life of 10-12 days for PKH67. Other green cell linker dyes with similar half lives have been used to monitor in vivo lymphocyte and macrophage trafficking over periods of 1-2 months, suggesting that PKH67 will also be useful for in vivo tracking studies of moderate length.
결합
법적 정보
키트 구성품 전용
- Diluent C 6 x 10
- PKH67 Cell Linker in ethanol .5 mL
관련 제품
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
Flash Point (°F)
57.2 °F - closed cup
Flash Point (°C)
14 °C - closed cup
이미 열람한 고객
문서
PKH dyes are easy to use and achieve stable, uniform, and reproducible fluorescent labeling of live cells. PKH dyes are non-toxic membrane stains which produce high signal to noise ratio.
Lipophilic cell tracking dyes enable cancer biologists to track tumor and immune cell functions both in vitro and in vivo. Read the article to choose a right membrane dye kit for cell tracking and proliferation monitoring.
Optimal staining is a key component for studying tumorigenesis and progression. Learn useful tips and techniques for dye applications, including examples from recent studies.
PKH and CellVue® Fluorescent Cell Linker Kits provide fluorescent labeling of live cells over an extended period of time, with no apparent toxic effects.
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I mark mitochondria for injection with PKH26 Red Fluorescent Cell Linker Kit for General Cell Membrane Labeling. I want to use another dye to mark another type of mitochondria and inject them together in the same fish egg. Is PKH67 ok for this like PKH26?
1 답변-
도움이 되었습니까?
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What can be the alternative for removing excess dye after labeling of exosomes using PKH67 dye apart from ultracentrifugation?
1 답변-
Excess dye is bound to serum or albumin which is added to the cell/dye mixture as a stop reaction. The recommended clean up or dye removal is by standard centrifugation (400 x g for 10 minutes, wash, and repeat). See the Product Information Sheet, page 3, bullet point 8 for more information:
https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/984/984/pkh67glbul.pdfAlternate methods for excess dye removal have not been investigated.
도움이 되었습니까?
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Can we remove the excess PKH67 DYE used for the labeling of exosomes using exosome spin column rather than ultracentrifugation.
1 답변-
The recommended exosome labeling protocol has been optimized to assure the best possible results. The use of exosome spin columns with the PKH and CellVue products has not been validated. See below for a link to our exosome labeling protocol. A spin column method may not offer the best results.
도움이 되었습니까?
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Will Product PKH67, Green Fluorescent Cell Linker Kit, stain dead cells?
1 답변-
As long as the cell has an intact membrane, the PKH76 dye can label the cell.
도움이 되었습니까?
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What is the difference between Green Fluorescent Cell Linker Kits PKH2 and PKH67?
1 답변-
PKH2 was one of the early PKH dyes. The PKH67 dye has a longer aliphatic tail. There is reduced cell-celldye transfer for PKH67 as compared with PKH2.
도움이 되었습니까?
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What method of fixation can be used for tissue/cells with the PKH Fluorescent Cell Linker Kit for General Cell Membrane Labeling dyes?
1 답변-
A protocol for visualization of tissue sections can be found in the technical bulletin. For visualization of stained cells by immunofluorescence or flow cytometry, the cells can be fixed in 2% paraformaldehyde for 15 minutes. The use of other organic solvents will extract the dye from the cells. If internal labeling is desired, the cells can be permeabilized with saponin (50-75 μg/mL). Here is the link to the Troubleshooting Guide.
도움이 되었습니까?
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What is the Department of Transportation shipping information for this product?
1 답변-
Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
도움이 되었습니까?
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What is the excitation and emission spectra for Product PKH67GL, Green Fluorescent Cell Linker Kit?
1 답변-
The spectra can be found on the product insert.The product has a maximum excitation at 490 nm and maximum emission at 502 nm.
도움이 되었습니까?
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How many cells can be stained with Product PKH67GL, Green Fluorescent Cell Linker Kit?
1 답변-
This kit can stain 50 × 107 cells if used as directed (1 × 107 cells stained with 2 × 10-6 M PKH67).
도움이 되었습니까?
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When using Product PKH67GL, PKH67 Green Fluorescent Cell Linker Kit for General Cell Membrane Labeling, how long will the cells remain stained after treatment?
1 답변-
Labeled cells that have been washed can be visualized in culture up to 100 days after staining (for non-dividing cells). The dye itself is stable and will divide equally when the cells divide. After staining with PKH dyes, you can observe as many as 8 divisions depending on how brightly the cells were stained initially and the amount of surface area on the cells. Most commonly, 4-6 divisions can be visualized.
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