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인용 및 참조 문헌 (27)
Invitrogen™
Magnesium Green™, Pentapotassium Salt, cell impermeant
The cell-impermeant Magnesium Green™, potassium salt exhibits a higher affinity for Mg2+ (Kd ∼1.0 mM) than mag-fura-2 (Kd ∼1.9 mM)자세히 알아보기
| 카탈로그 번호 | 수량 |
|---|---|
| M3733 | 1 mg |
카탈로그 번호 M3733
제품 가격(KRW)
538,000
온라인 행사
Ends: 31-Mar-2026
614,000할인액 76,000 (12%)
Each
수량:
1 mg
제품 가격(KRW)
538,000
온라인 행사
Ends: 31-Mar-2026
614,000할인액 76,000 (12%)
Each
The cell-impermeant Magnesium Green™, potassium salt exhibits a higher affinity for Mg2+ (Kd ∼1.0 mM) than mag-fura-2 (Kd ∼1.9 mM) or mag-indo-1 (Kd ∼2.7 mM). Upon binding Mg2+, Magnesium Green exhibits and increase in fluorescence emission intensity without a shift in wavelength with absorption/emission maxima ∼506/531 nm.
Learn more about ion indicators including calcium, potassium, pH, and membrane potential indicators ›
Learn more about ion indicators including calcium, potassium, pH, and membrane potential indicators ›
For Research Use Only. Not for use in diagnostic procedures.
사양
검출 방법Fluorescence
염료 유형Magnesium Indicator
수량1 mg
배송 조건Room Temperature
용도 (장비)Fluorescence Microscope, Microplate Reader
제품라인Magnesium Green
제품 유형Pentapotassium Salt
Unit SizeEach
구성 및 보관
Store in freezer -5°C to -30°C and protect from light.
인용 및 참조 문헌 (27)
인용 및 참조 문헌
Abstract
Presynaptic Ca(2+) influx at the inhibitor of the crayfish neuromuscular junction: a photometric study at a high time resolution.
Journal:J Neurophysiol
PubMed ID:10634895
'Presynaptic calcium influx at the inhibitor of the crayfish neuromuscular junction was investigated by measuring fluorescence transients generated by calcium-sensitive dyes. This approach allowed us to correlate presynaptic calcium influx with transmitter release at a high time resolution. Systematic testing of the calcium indicators showed that only low-affinity dyes, with
Requirement for an additional divalent metal cation to activate protein tyrosine kinases.
Journal:Biochemistry
PubMed ID:9047313
'In addition to the magnesium ion needed to form the true phosphate-donating substrate (ATP-Mg complex), we have determined that at least one additional Mg2+ ion is essential for the activation of protein tyrosine kinases. This activation was investigated in detail using purified Csk, Src, and the fibroblast growth factor receptor
Ca2+ fluorescence imaging with pico- and femtosecond two-photon excitation: signal and photodamage.
Journal:Biophys J
PubMed ID:10512842
'The signal and limitations of calcium florescence imaging using nonresonant multiphoton absorption of near-infrared femto- and picosecond laser pulses were examined. The fluorescence changes of various Ca(2+)-indicators induced by transient increases of the intradendritic calcium concentration were evaluated by evoking physiological activity in neocortical neurons in rat brain slices. Photodamage
Effects of magnesium on cyclic GMP hydrolysis by the bovine retinal rod cyclic GMP phosphodiesterase.
Journal:Biochem J
PubMed ID:7772055
'Knowledge of the kinetics of the rod cyclic GMP phosphodiesterase is essential for understanding the kinetics and gain of the light response. Therefore, the interactions between Mg2+, cyclic GMP, and purified, trypsin-activated bovine rod cyclic GMP phosphodiesterase (EC 3.1.4.17) were examined. The effects of Mg2+ and of cyclic GMP on
Mechanisms of calcium influx into hippocampal spines: heterogeneity among spines, coincidence detection by NMDA receptors, and optical quantal analysis.
Journal:J Neurosci
PubMed ID:10066251
'Dendritic spines receive most excitatory inputs in the vertebrate brain, but their function is still poorly understood. Using two-photon calcium imaging of CA1 pyramidal neurons in rat hippocampal slices, we investigated the mechanisms by which calcium enters into individual spines in the stratum radiatum. We find three different pathways for