Passa al contenuto
Merck
Tutte le immagini(1)

Documenti fondamentali

Visualizza tutta la documentazione

39294

Sigma-Aldrich

Fluo 3-AM solution

1 mM in DMSO, ≥99.0% (TLC)

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula empirica (notazione di Hill):
C51H50Cl2N2O23
Numero CAS:
121714-22-5
Peso molecolare:
1129.85
Numero MDL:
MFCD00083336
Codice UNSPSC:
12171500
NACRES:
NA.32

Saggio

≥99.0% (TLC)

Stato

liquid

Concentrazione

1 mM in DMSO

Fluorescenza

λex 506 nm; λem 525.0 nm±5.0 nm in 0.1 M Tris pH 8.0, esterase

Temperatura di conservazione

−20°C

Stringa SMILE

Clc1[c](cc2[o]c3c(c(c2c1)c4cc(c(cc4)N(CC(=O)OCOC(=O)C)CC(=O)OCOC(=O)C)OCCOc5c(ccc(c5)C)N(CC(=O)OCOC(=O)C)CC(=O)OCOC(=O)C)cc(c(c3)OCOC(=O)C)Cl)=O

InChI

1S/C51H50Cl2N2O23/c1-28-7-9-39(54(19-47(62)74-24-69-30(3)57)20-48(63)75-25-70-31(4)58)45(13-28)66-11-12-67-46-14-34(8-10-40(46)55(21-49(64)76-26-71-32(5)59)22-50(65)77-27-72-33(6)60)51-35-15-37(52)41(61)17-42(35)78-43-18-44(38(53)16-36(43)51)73-23-68-29(2
PTPUOMXKXCCSEN-UHFFFAOYSA-N

Descrizione generale

Cell permeable fluorescent indicator of intracellular Ca2+; non-fluorescent until it is hydrolyzed intracellularly and/or in the presence of Ca2+; lower binding affinity allows measurement of higher peaks of Ca2+ transients than with Fura 2.

Applicazioni

suitable as fluorescent Ca sensitive probe (after cleavage of the AM ester)

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

188.6 °F

Punto d’infiammabilità (°C)

87 °C

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCG6962
BCCB4646
BCBV3584
BCBP7162V
BCBP1596V

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 5

1 of 5

BAPTA-AM ≥95% (HPLC)

Sigma-Aldrich

A1076

BAPTA-AM

Polyvinyl alcohol mounting medium with DABCO®, antifading pH 8.7

Supelco

10981

Polyvinyl alcohol mounting medium with DABCO®, antifading

Calcium Ionophore A23187 ≥98% (TLC), powder

Sigma-Aldrich

C7522

Calcium Ionophore A23187

Chlortetracycline hydrochloride ≥91.0% dry basis (HPLC)

Sigma-Aldrich

C4881

Chlortetracycline hydrochloride

Calcein AM solution 4 mM in DMSO, ≥90% (HPLC), solution

Sigma-Aldrich

C1359

Calcein AM solution

Shiwen Han et al.
Scientific reports, 7(1), 7222-7222 (2017-08-05)
Glycyrrhizic acid (GA), the major bioactive triterpene glycoside of glycyrrhiza, has been shown to possess a wide range of pharmacological properties, including anti-inflammatory and anti-viral properties. However, few studies have examined the anti-allergic activity and exact mechanism of action of
Tamagno Pesqueira et al.
Scientific reports, 7(1), 10948-10948 (2017-09-10)
Magnetotherapy has been receiving increased attention as an attractive strategy for modulating cell physiology directly at the site of injury, thereby providing the medical community with a safe and non-invasive therapy. Yet, how magnetic field influences tendon cells both at
Yueliang Zhao et al.
Food & function, 10(5), 2729-2738 (2019-05-01)
Brosimone I is an isoprenoid-substituted flavonoid from Artocarpus heterophyllus. Here, we reported for the first time that brosimone I induced cell cycle G1 phase arrest and apoptosis in HCT116 human colon cancer cells. Brosimone I treatment increased the cytosolic Ca2+
Shrawan Kumar Mishra et al.
Biochimica et biophysica acta. Molecular and cell biology of lipids, 1864(2), 158-167 (2018-11-26)
Human GLTP on chromosome 12 (locus 12q24.11) encodes a 24 kD amphitropic lipid transfer protein (GLTP) that mediates glycosphingolipid (GSL) intermembrane trafficking and regulates GSL homeostatic levels within cells. Herein, we provide evidence that GLTP overexpression inhibits the growth of
Ruo-Xiao Cheng et al.
Theranostics, 9(15), 4287-4307 (2019-07-10)
Methylglyoxal (MGO), an endogenous reactive carbonyl compound, plays a key role in the pathogenesis of diabetic neuropathy. The aim of this study is to investigate the role of MGO in diabetic itch and hypoalgesia, two common symptoms associated with diabetic

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.