Escherichia coli (K-12 strain) BioParticles™, Alexa Fluor™ 488 conjugate
<i>Escherichia coli</i> (K-12 strain) BioParticles&trade;, Alexa Fluor&trade; 488 conjugate
Invitrogen™

Escherichia coli (K-12 strain) BioParticles™, Alexa Fluor™ 488 conjugate

Molecular Probes™ BioParticles™製品ラインは、さまざまなサイズ、形状、および天然の抗原性で、蛍光標識され、熱または化学的に死滅させられた細菌および酵母で構成されています。これらの蛍光BioParticles™製品は、蛍光顕微鏡法詳細を見る
製品番号(カタログ番号)数量
E132312 mg
製品番号(カタログ番号) E13231
価格(JPY)
49,800
Each
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数量:
2 mg
Ask our AI about this Product
Molecular Probes™ BioParticles™製品ラインは、さまざまなサイズ、形状、および天然の抗原性で、蛍光標識され、熱または化学的に死滅させられた細菌および酵母で構成されています。これらの蛍光BioParticles™製品は、蛍光顕微鏡法、定量的分光光度法、およびフローサイトメトリーによる食作用の研究に使用されています。

当社は、大腸菌(K-12株)、黄色ブドウ球菌(タンパク質Aを含まない木材株)、およびザイモサン(出芽酵母)BioParticles™コンジュゲートをさまざまな蛍光色素で共有標識して提供しています(結合後に遊離色素を除去するために特別な注意が必要です)。酸性環境で部分的に消光される蛍光標識BioParticles™コンジュゲートの蛍光とは異なり、Alexa Fluor™、BODIPY™ FL、テトラメチルローダミン、Texas Red™色素コンジュゲートは、3〜10のpH範囲で均一に強い蛍光を示します。

BioParticlesの仕様:
• 標識(Ex/Em):Alexa Fluor™ 488 (∼495/519 nm)
• 粒子:大腸菌(K-12株)
オプソニン試薬が利用可能


BioParticles製品の使用について
BioParticles™コンジュゲートは凍結乾燥粉末として提供されます。約3 x 108の大腸菌または黄色ブドウ球菌粒子/mg(固体)および約2 x 107のザイモサン粒子/mg(固体)が存在します。BioParticles™コンジュゲートは、食作用アッセイで使用するために選択した緩衝液で再構成できます。細胞の表面に結合している(しかし内部に取り込まれていない)BioParticles™コンジュゲートの蛍光は、エチジウムブロマイド、トリパンブルー、または他のクエンチャーよって消光できます。細胞での用途に加えて、蛍光BioParticles™コンジュゲートは、細菌や酵母変異体を分類する際のフローサイトメトリーキャリブレーションリファレンスとして有効な場合があります。微小粒子は、サイズと形状が特徴的に異なるため、光散乱研究の参考になる可能性もあります。

その他のBioParticles™製品
当社は、色素標識および非標識の大腸菌(K-12株)、黄色ブドウ球菌(タンパク質Aを含まない木材株)、およびザイモサン(出芽酵母)BioParticles™製品を幅広く提供しています。これらの製品とその用途については、「Molecular Probes™ハンドブック」の受容体結合と食作用を追跡するためのプローブ — セクション16.1を参照してください。

pH感受性が高いエンドサイトーシスアッセイについては、当社のpHrodo™ BioParticles™コンジュゲートを参照してください。

本製品は研究用試薬です。ヒトまたは動物の治療もしくは診断目的には使用できません。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
細胞タイプMammalian Cell
検出法蛍光
染色剤タイプAlexa Fluor™ 488
形状固体
数量2 mg
出荷条件室温
E. coli
使用対象 (装置)Fluorescence Microscope
製品ラインAlexa Fluor™、BioParticles™
製品タイプ大腸菌コンジュゲート
Unit SizeEach
組成および保存条件
フリーザー(-5~-30度)に保存し、遮光してください。
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蛍光スペクトル

Fluorescence spectra

ドキュメントおよびダウンロード

証明書

ロット番号Certificate TypeDateCatalog Number(s)
2978772Certificate of Analysis2024年8月06日E13231
2752572Certificate of Analysis2023年12月06日E13231
2415922Certificate of Analysis2021年12月16日E13231
2311805Certificate of Analysis2021年7月13日E13231
2260953Certificate of Analysis2020年12月16日E13231
5件の結果が表示されました。 上記から特定の証明書を検索します

Safety Data Sheets

よくあるご質問(FAQ)

The Escherichia coli (K-12 strain) BioParticles, Alexa Fluor 488 conjugate are supplied as lyophilized powder in a 2 mg unit size. There are approximately 3 x 10E8 E. coli particles per mg solid.

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

The particle size of Escherichia coli (K-12 strain) BioParticles fluorescent conjugates are approximately 0.2 micron wide and 2-3 micron long.

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

While the bacteria have been attenuated with formaldehyde and alcohol desiccation, the BioParticles products are not considered sterile, and we do not recommend incubation of more than 4 hours. This applies to all of our dye-labeled (pHrodo, Alexa Fluor, etc.) and unlabeled BioParticles products.

We use amine-reactive dyes to covalently attach fluorescent dyes to all of our BioParticles probes such as the Escherichia coli (K-12 strain) BioParticles probes, Staphylococcus aureus (Wood strain without protein A) BioParticles, and the Zymosan A (S. cerevisiae) BioParticles probes.

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

-Calcium flux: Each of the Oregon Green calcium indicators binds intracellular calcium with increasing affinity, providing a sensitivity range to match many applications. Oregon Green probes emit green fluorescence at resting levels of Ca2+ and increase their fluorescence intensity 14-fold with increasing Ca2+ concentration. The cell-permeant formulation (Cat. No. O6807) can be loaded in cell media and is compatible with flow cytometry.
-Rhodamine-based calcium indicators comprise a range of probes for large or small changes in Ca2+ concentration. They exhibit a 50-fold increase in fluorescence upon calcium binding and offer a range of wavelengths that can be used in conjunction with GFP or green-fluorescent dyes for multiplexing. Rhod-2, AM (Cat. No. R1245MP), in particular, localizes to mitochondria and can be used with flow cytometry.
-Membrane potential: A distinctive feature of the early stages of apoptosis is the disruption of the mitochondria, including changes in membrane and redox potential. We offer a range of products specifically designed to assay mitochondrial membrane potential in live cells by flow cytometry, with minimal disruption of cellular function. The MitoProbe family of mitochondrial stains (Cat. Nos. M34150, M34151, and M34152) provide quick, easy, and reliable flow cytometric detection of the loss of mitochondrial membrane potential that occurs during apoptosis. MitoTracker dyes (Cat. Nos. M7510 and M7512) are membrane potential-dependent probes for staining mitochondria in live cells. The staining pattern of MitoTracker dyes is retained throughout subsequent flow cytometry immunocytochemistry, DNA end labeling, in situ hybridization, or counterstaining steps. The Mitochondrial Permeability Transition Pore Assay (Cat. No. M34153) provides a more direct method of measuring mitochondrial permeability transition pore opening than assays relying on mitochondrial membrane potential alone. The mitochondrial permeability transition pore (MPTP) is a non-specific channel formed by components from the inner and outer mitochondrial membranes, and appears to be involved in the release of mitochondrial components during cell death.
-Phagocytosis: In phagocytosis, cells internalize particulate matter such as microorganisms, and this process is important for immune responses and during the clearance of apoptotic cells. Probes for studying phagocytosis include BioParticles indicators—bacteria and yeast labeled with fluorescent dyes.
-Tracking phagocytosis using a quench/wash-based assay can report on simple uptake, or a pH indicator can be used to monitor stages in the pathway. We have no-wash assays labeled with pHrodo Red or Green (Cat. Nos. A10010, P35361, P35364, P35365, P35366, and P35367) and no-wash assays for whole blood (Cat. Nos. A10025, A10026, P35381, and P35382), all suitable for flow cytometry.
-pH changes: Sensitive pH determinations can be made in a physiological range using either fluorescent intensity or ratiometric measurements. pHrodo dyes (Cat. Nos. P35373 and P35372) provide signal intensity modulation from pH 2 to pH 9 and with a choice of fluorescent wavelengths. Tracking internalization of fluorescent dextran is a routine method for analyzing pH changes in cellular compartments. Dextran conjugates of pHrodo dyes (Cat. Nos. P35368 and P10361) provide the most complete solution by allowing discrimination of vesicles from early endosomes to lysosomes, with no quench or wash required.
-Reactive oxygen species: Cells that are environmentally stressed usually contain greatly increased levels of reactive oxygen species (ROS). CellROX reagents are fluorogenic probes developed for the detection and quantitation of ROS in live cells. These cell-permeant reagents are non-fluorescent or very weakly fluorescent in the reduced state; however, when oxidized, they become brightly fluorescent and remain localized within the cell. We offer CellROX Green (Cat. No. C10492), CellROX Orange (Cat. No. C10493), and CellROX Deep Red (Cat. No. C10491) Assay Kits validated for flow cytometry.

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

引用および参考文献 (6)

引用および参考文献
Abstract
Extracellular Matrix Lumican Promotes Bacterial Phagocytosis, and Lum-/- Mice Show Increased Pseudomonas aeruginosa Lung Infection Severity.
Authors:Shao H, Lee S, Gae-Scott S, Nakata C, Chen S, Hamad AR, Chakravarti S,
Journal:J Biol Chem
PubMed ID:22865855
'Phagocytosis is central to bacterial clearance, but the exact mechanism is incompletely understood. Here, we show a novel and critical role for lumican, the connective tissue extracellular matrix small leucine-rich repeat proteoglycan, in CD14-mediated bacterial phagocytosis. In Psuedomonas aeruginosa lung infections, lumican-deficient (Lum(-/-)) mice failed to clear the bacterium from ... More
Multipotent stem cells from trabecular meshwork become phagocytic TM cells.
Authors:Du Y, Roh DS, Mann MM, Funderburgh ML, Funderburgh JL, Schuman JS,
Journal:Invest Ophthalmol Vis Sci
PubMed ID:22297497
'To isolate and characterize stem cells from human trabecular meshwork (TM) and to investigate the potential of these stem cells to differentiate into TM cells. Human trabecular meshwork stem cells (TMSCs) were isolated as side population cells by fluorescence-activated cell sorting or isolated by clonal cultures. Passaged TMSCs were compared ... More
Antibody to Langerin/CD207 localizes large numbers of CD8alpha+ dendritic cells to the marginal zone of mouse spleen.
Authors:Idoyaga J, Suda N, Suda K, Park CG, Steinman RM,
Journal:Proc Natl Acad Sci U S A
PubMed ID:19168629
Dendritic cells (DCs) are strategically positioned to take up antigens and initiate adaptive immunity. One DC subset expresses CD8alphaalpha in mice and is specialized to capture dying cells and process antigens for MHC class I  ... More
PLD$ is involved in phagocytosis of microglia: expression and localization changes of PLD4 are correlated with activation state of microglia.
Authors:Otani Y, Yamaguchi Y, Sato Y, Furuichi T, Ikenaka K, Kitani H, Baba H,
Journal:PLoS One
PubMed ID:22102906
Phospholipase D4 (PLD4) is a recently identified protein that is mainly expressed in the ionized calcium binding adapter molecule 1 (Iba1)-positive microglia in the early postnatal mouse cerebellar white matter. Unlike PLD1 and PLD2, PLD4 exhibits no enzymatic activity for conversion of phosphatidylcholine into choline and phosphatidic acid, and its ... More
Live cell imaging of zebrafish leukocytes.
Authors:Hall C, Flores MV, Crosier K, Crosier P,
Journal:Methods Mol Biol
PubMed ID:19378109
Zebrafish are ideally suited for the live imaging of early immune cell compartments. Macrophages that initially appear on the yolk surface prior to the onset of circulation are the first functional immune cells within the embryo, predating the emergence of the first granulocytic cells-the heterophilic neutrophils. Both cell types have ... More
6 total citations

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