Oregon Green™ 488 BAPTA-1, AM, cell permeant - Special Packaging
Oregon Green™ 488 BAPTA-1, AM, cell permeant - Special Packaging
Invitrogen™

Oregon Green™ 488 BAPTA-1, AM, cell permeant - Special Packaging

표지된 칼슘 표지자(calcium indicator)는 Ca2+ 결합 시 형광이 증강되는 분자입니다. 살아있는 조직에서 Ca2+ 의 유입 및 방출 후 세포자세히 알아보기
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카탈로그 번호수량
O680710 x 50 μg
카탈로그 번호 O6807
제품 가격(KRW)
632,000
온라인 행사
Ends: 31-Mar-2026
722,000
할인액 90,000 (12%)
Each
카트에 추가하기
수량:
10 x 50 μg
제품 가격(KRW)
632,000
온라인 행사
Ends: 31-Mar-2026
722,000
할인액 90,000 (12%)
Each
카트에 추가하기
표지된 칼슘 표지자(calcium indicator)는 Ca2+ 결합 시 형광이 증강되는 분자입니다. 살아있는 조직에서 Ca2+ 의 유입 및 방출 후 세포 내 Ca2+ 측정 및 Ca2+의 multiphoton excitation imaging 등 여러 가지 칼슘 신호전달 연구에 사용할 수 있습니다. 용해된 표지자를 세포 배양 접시에 직접 첨가하여 이런 칼슘 표지자의 AM ester 형을 세포에 loading할 수 있습니다. 이런 세포에서 형광 신호는 대개 fluorescence microscopy, fluorescence microplate assay 또는 flow cytometry로 측정됩니다.

Calcium 표지자(AM Ester) 사양:
• Label (Ex/Em): Oregon Green™ 488 BAPTA-1 (494/523 nm)
• Ca2+ 결합 시 형광 강도가 높아집니다 (∼14배).
• Ca2+ 결합 시 파장의 변화는 거의 없이 형광 증가가 나타납니다.


Molecular Probes™ Calcium 표지자의 분광 특징
이들 probe는 가시광선으로 여기(excitation)되며 여기에 필요한 에너지가 낮기 때문에 세포 광손상 가능성이 적습니다. 흔히 사용되는 레이저 기반 기기(예. confocal laser scanning microscope)가 이런 표지자를 효율적으로 여기시킬 수 있으며 세포 자가형광(autofluroscence) 및 분산(scattering) background가 거의 문제가 되지 않는 스펙트럼 영역에서 emission이 일어납니다.

그 밖의 Fluorescent Calcium 표지자 선택
본사는 다양한 실험 조건에 사용할 수 있도록 누출 감소 및 compartmentalization를 위한 dextran 버전, high-amplitude calcium transients 검출을 위한 BAPTA conjugate 등 다양한 Molecular Probes™ calcium 표지자를 제공합니다. 자세한 정보는 Molecular Probes™ 핸드북에서 가시광선 여기 형광 Ca2+ 표지자—Section 19.3을 참조하십시오.

UV 여기 Ca2+ 표지자, 단백질 기반 Ca2+ 표지자, Ca2+ conjugate 표지자, 기타 금속 이온(i.e., Mg2+, Zn2+)의 형광 기반 표지자는 Molecular Probes™ 핸드북에서 Ca2+, Mg2+, Zn2+ 및 기타 금속 이온 표지자—Chapter 19를 참조하십시오.

연구용으로만 사용할 수 있습니다. 동물이나 사람의 치료 또는 진단 목적으로 사용할 수 없습니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
검출 방법Fluorescence
염료 유형Fluorescent Dye-Based
수량10 x 50 μg
배송 조건Room Temperature
용도(애플리케이션)Cell Viability and Proliferation
용도 (장비)Fluorescence Microscope, Flow Cytometer, Microplate Reader
제품라인Oregon Green
제품 유형Stain
Unit SizeEach
구성 및 보관
Store in freezer -5°C to -30°C.

자주 묻는 질문(FAQ)

What cellular processes can be analyzed with a flow cytometer?

-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.

인용 및 참조 문헌 (129)

인용 및 참조 문헌
Abstract
Normal fertilization occurs with eggs lacking the integrin alpha6beta1 and is CD9-dependent.
Authors:Miller BJ, Georges-Labouesse E, Primakoff P, Myles DG
Journal:J Cell Biol
PubMed ID:10851025
'Previous results, based on inhibition of fertilization by an anti-alpha6 integrin mAb (GoH3), suggest that the alpha6beta1 integrin on mouse eggs functions as the receptor for sperm (Almeida, E.A., A.P. Huovila, A.E. Sutherland, L.E. Stephens, P.G. Calarco, L. M. Shaw, A.M. Mercurio, A. Sonnenberg, P. Primakoff, D.G. Myles, and J.M. ... More
Acetylcholine-induced calcium signaling and contraction of airway smooth muscle cells in lung slices.
Authors:Bergner A, Sanderson MJ
Journal:J Gen Physiol
PubMed ID:11815668
'The Ca(2+) signaling and contractility of airway smooth muscle cells (SMCs) were investigated with confocal microscopy in murine lung slices (approximately 75-microm thick) that maintained the in situ organization of the airways and the contractility of the SMCs for at least 5 d. 10--500 nM acetylcholine (ACH) induced a contraction ... More
Intracellular astrocyte calcium waves in situ increase the frequency of spontaneous AMPA receptor currents in CA1 pyramidal neurons.
Authors:Fiacco TA, McCarthy KD
Journal:J Neurosci
PubMed ID:14736858
'Spontaneous neurotransmitter release and activation of group I metabotropic glutamate receptors (mGluRs) each play a role in the plasticity of neuronal synapses. Astrocytes may contribute to short- and long-term synaptic changes by signaling to neurons via these processes. Spontaneous whole-cell AMPA receptor (AMPAR) currents were recorded in CA1 pyramidal cells ... More
The sources and sequestration of Ca(2+) contributing to neuroeffector Ca(2+) transients in the mouse vas deferens.
Authors:Brain KL, Cuprian AM, Williams DJ, Cunnane TC
Journal:J Physiol
PubMed ID:14500773
'The detection of focal Ca(2+) transients (called neuroeffector Ca(2+) transients, or NCTs) in smooth muscle of the mouse isolated vas deferens has been used to detect the packeted release of ATP from nerve terminal varicosities acting at postjunctional P2X receptors. The present study investigates the sources and sequestration of Ca(2+) ... More
Control of IP(3)-mediated Ca2+ puffs in Xenopus laevis oocytes by the Ca2+-binding protein parvalbumin.
Authors:John LM, Mosquera-Caro M, Camacho P, Lechleiter JD
Journal:J Physiol
PubMed ID:11507154
'1. Elementary events of Ca2+ release (Ca2+ puffs) can be elicited from discrete clusters of inositol 1,4,5 trisphosphate receptors (IP(3)Rs) at low concentrations of IP(3). Ca(2+) puffs have rarely been observed unless elicited by either hormone treatment or introduction of IP(3) into the cell. However, cells appear to have sufficient ... More