BODIPY™ 493/503(4,4-二氟-1,3,5,7,8-五甲基-4-硼杂-3a,4a-二氮杂-s-引达省)
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BODIPY&trade; 493/503(4,4-二氟-1,3,5,7,8-五甲基-4-硼杂-3a,4a-二氮杂-<i>s</i>-引达省)
Invitrogen™

BODIPY™ 493/503(4,4-二氟-1,3,5,7,8-五甲基-4-硼杂-3a,4a-二氮杂-s-引达省)

BODIPY™ 493/503 具有非极性结构、吸收波长较长且发荧光,可作为中性脂质染色剂及油和其他非极性脂质的示踪剂。我们建议在优质无水 DMSO 中溶解以达到1至 10 mM 的储备液浓度了解更多信息
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货号数量
D392210 mg
货号 D3922
价格(CNY)
3,095.00
飞享价
Ends: 31-Dec-2025
4,195.00
共减 1,100.00 (26%)
Each
添加至购物车
数量:
10 mg
价格(CNY)
3,095.00
飞享价
Ends: 31-Dec-2025
4,195.00
共减 1,100.00 (26%)
Each
添加至购物车
BODIPY™ 493/503 具有非极性结构、吸收波长较长且发荧光,可作为中性脂质染色剂及油和其他非极性脂质的示踪剂。我们建议在优质无水 DMSO 中溶解以达到1至 10 mM 的储备液浓度。

仅供科研使用。不可用于诊断程序。
规格
激发/发射493/504 nm
标签类型BODIPY 染料
分子式C14H17BF2N2
产品线BODIPY
数量10 mg
建议的储存条件在冷冻冰箱(-5°C 至 -30°C)中避光储存。
运输条件室温
物理形态实心
产品类型脂肪酸
Unit SizeEach

常见问题解答 (FAQ)

What is the difference between BODIPY 493/503 (4,4-Difluoro-1,3,5,7,8-Pentamethyl-4-Bora-3a,4a-Diaza-s-Indacene) (Cat. No. D3922) and BODIPY 493/503 NHS Ester (Succinimidyl Ester) (Cat. No. D2191)?

BODIPY 493/503 NHS Ester (Succinimidyl Ester) (Cat. No. D2191) is the amine‐reactive derivative of BODIPY 493/503 (4,4‐Difluoro‐1,3,5,7,8‐Pentamethyl‐4‐Bora‐3a,4a‐Diaza‐s‐Indacene) (Cat. No. D3922). The reactive group allows for D2191 to be used as a labeling reagent to label proteins or other molecules to covalently attach the dye to accessible primary amines. If using this as a live cell reagent, the reactive group may allow for better retention as it will covalently attach to any primary amines on any cellular material it may come into contact with.

Find additional tips, troubleshooting help, and resources within our Cell Imaging Support Center.

Do you have protocol information for use of BODIPY 493/503 (Cat. No. D3922) on paraffin section?

We do not have a protocol for using BODIPY 493/503 (D3922) on paraffin section. This product is typically used on live cells.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

How can I stain live cells with Invitrogen BODIPY 493/503 dye (Cat. No.D3922)?

Invitrogen BODIPY 493/503 dye (Cat no. D3922) being a hydrophobic dye does not disperse readily into aqueous solutions. To consistently stain cells with this dye, follow this protocol:

- Place your cells in a half-volume of buffer or media. For this example, if you have 1x10E6 cells/mL in 1 mL, place them as 1x10E6 cells into a 0.5 mL volume (2x10E6 cells/mL).
- Make a 2X solution of Invitrogen BODIPY 493/503 dye in 0.5 mL volume of the same pre-warmed buffer or media (no cells, no BSA or serum) and mix vigorously to mechanically emulsify this solution.
- Either vortex, sonicate or shake vigorously by hand and then IMMEDIATELY add this to the solution of cells and then mix or roll gently.
- For adherent cells, swirl gently or pipette up and down.
- When the 0.5 mL of the 2X dye/buffer solution is added to the 0.5 mL of cells/buffer, the final dye concentration will be 1X and the cells will be at their appropriate final density of 1x10E6 cells/mL.

Final dye concentrations can range from 1 to 10 µM with incubation times ranging from a few mins up to 30 mins; the optimal final concentration and incubation times should be optimized per the application.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

What can be used to make a stock solution of Invitrogen BODIPY 493/503 dye (Cat. No. D3922)?

For Invitrogen BODIPY 493/503 dye (Cat. No. D3922), one may make a stock solution of 3.8 mM (1 mg/mL) in high-quality anhydrous DMSO. After resolubilizing, store the stock solution frozen, desiccated, and protected from the light. Solutions up to 1mM can also be made in absolute ethanol.

Please note that both the DMSO and ethanol should be of high quality and anhydrous or the compound may not dissolve.

For long-term storage, dissolve the dye at 1 mM using absolute ethanol, make smaller aliquots in separate vials, and then evaporate off the ethanol using a vacuum pump. Store the solid dye frozen and protected from the light.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

引用和文献 (54)

引用和文献
Abstract
Functional analysis of FSP27 protein regions for lipid droplet localization, caspase-dependent apoptosis, and dimerization with CIDEA.
Authors:Liu K, Zhou S, Kim JY, Tillison K, Majors D, Rearick D, Lee JH, Fernandez-Boyanapalli RF, Barricklow K, Houston MS, Smas CM,
Journal:Am J Physiol Endocrinol Metab
PubMed ID:19843876
'The adipocyte-specific protein FSP27, also known as CIDEC, is one of three cell death-inducing DFF45-like effector (CIDE) proteins. The first known function for CIDEs was promotion of apoptosis upon ectopic expression in mammalian cells. Recent studies in endogenous settings demonstrated key roles for CIDEs in energy metabolism. FSP27 is a ... More
Regulated localization of Rab18 to lipid droplets: effects of lipolytic stimulation and inhibition of lipid droplet catabolism.
Authors:Martin S, Driessen K, Nixon SJ, Zerial M, Parton RG
Journal:J Biol Chem
PubMed ID:16207721
'Rab GTPases are crucial regulators of membrane traffic. Here we have examined a possible association of Rab proteins with lipid droplets (LDs), neutral lipid-containing organelles surrounded by a phospholipid monolayer, also known as lipid bodies, which have been traditionally considered relatively inert storage organelles. Although we found close apposition between ... More
High glucose induces adipogenic differentiation of muscle-derived stem cells.
Authors:Aguiari P, Leo S, Zavan B, Vindigni V, Rimessi A, Bianchi K, Franzin C, Cortivo R, Rossato M, Vettor R, Abatangelo G, Pozzan T, Pinton P, Rizzuto R,
Journal:Proc Natl Acad Sci U S A
PubMed ID:18212116
'Regeneration of mesenchymal tissues depends on a resident stem cell population, that in most cases remains elusive in terms of cellular identity and differentiation signals. We here show that primary cell cultures derived from adipose tissue or skeletal muscle differentiate into adipocytes when cultured in high glucose. High glucose induces ... More
Fixation methods for the study of lipid droplets by immunofluorescence microscopy.
Authors:DiDonato D, Brasaemle DL
Journal:J Histochem Cytochem
PubMed ID:12754288
'The study of proteins associated with lipid droplets in adipocytes and many other cells is a rapidly developing area of inquiry. Although lipid droplets are easily visible by light microscopy, few standardized microscopy methods have been developed. Several methods of chemical fixation have recently been used to preserve cell structure ... More
Spatial integration of TIP47 and adipophilin in macrophage lipid bodies.
Authors:Robenek H, Lorkowski S, Schnoor M, Troyer D
Journal:J Biol Chem
PubMed ID:15545278
'We studied the distribution of the PAT family proteins TIP47 and adipophilin in lipid bodies of THP-1 cell-derived macrophages using freeze-fracture immunolabeling and other techniques. Lipid bodies in macrophages comprise lipid droplets and extensive, previously scantily characterized sheet-like organelles, which we descriptively call "lipid sails." TIP47 and adipophilin are components ... More