Molecular Weight(MW): 764.68
BAPTA-AM is a selective, membrane-permeable calcium chelator.
Cited by 16 Publications
6 Customer Reviews
(A) Representative fluorescent images of co-localization of NLRP3 and mitochondria in NP cells as described in Figure 6C. Red and green fluorescence indicated NLRP3 and mitochondria signals, respectively. Cell nuclei are stained by DAPI. Representative fluorescent images of caspase-1 activity (B) in NP cells.
J Cell Mol Med, 2017, 21(7):1373-1387. BAPTA-AM purchased from Selleck.
BAPTA/AM and STO609 pretreatments did not inhibit BAM15-induced AMPK activation in A10 cells. A10 cells were treated with BAM15 (5 μmol/L, 5min) after BAPTA-AM (20 μmol/L, 1h) and STO-609 (50 μmol/L, 1 h) pretreatments. **P<0.01 vs DMSO (control).
Acta Pharm Sin B, 2018, 8(6):909-918. BAPTA-AM purchased from Selleck.
Formation of the AnxA2 complex in MBMECs was evaluated by immunoprecipitation and Western blot analysis after cryptococcal exposure. Endothelial cells were treated with PP2, BAPTA-AM, or DMSO (control) for 1 h before infection with cryptococcal cells and then rinsed twice with warm PBS. Lysates of infected or noninfected endothelial cells were preincubated with anti-AnxA2 Ab, and bound proteins were then blotted with anti-S100A10 Ab.
CNS Neurosci Ther, 2017, 23(4):291-300. BAPTA-AM purchased from Selleck.
Calcium chelator (BAPTA-AM) reduces HBV replication in CD36OE of HepG2.2.15 and HepAD38 cells. BAPTA-AM or vehicle controls (DMSO) were added to the CD36OE of HepG2.2.15 and HepAD38 cells for 96 h, and HBV DNA were extracted and detected by Real-time PCR (n = 4). Cytosolic Ca2+ was measured after treatment for 48 h using flow cytometry (n = 3).
Exp Cell Res, 2017, 358(2):360-368. BAPTA-AM purchased from Selleck.
A549 lung cancer cells were serum starved prior to treatment with TGF-β1 (10 ng/mL) or control for 12h in the presence or absence of BAPTA-AM (100μM). Protein expressions of Smad2/3, PSmad2 and P-Smad2 were detected by western blotting. (Values are shown as the mean ± SD. n=3, a representative experiment is shown; ‘*’means P<0.05)
Int J Biochem Cell Biol, 2017, 90:103-113. BAPTA-AM purchased from Selleck.
ER stress is necessary for MHBs-induced p38/NF-κB activation and an increase in IL-6. Huh7, L-02 and SMMC-7721 cells were transfected with MHB or GFP, the cells were treated with BAPTA-AM. (a) The phosphorylation of p38 MAPK and degradation of Iκ-B were detected by western blot.
PLoS One, 2016, 11(7):e0159089.. BAPTA-AM purchased from Selleck.
Purity & Quality Control
|Description||BAPTA-AM is a selective, membrane-permeable calcium chelator.|
BAPTA-AM, as an intracellular calcium chelator, induces delayed necrosis by lipoxygenase-mediated free radicals in mouse cortical cultures.  BAPTA-AM exerts an open channel blocking effect on hERG, hKv1.3 and hKv1.5 channels with IC50 of 1.3, 1.45 and 1.23 μM in HEK 293 cells. 
|In vivo||BAPTA-AM abolishes the UDCA- and TUDCA-induced increases in Ca2+ levels or Ca2+-Dependent PKC-α phosphorylation, and neutralizes the cytoprotective effects of UDCA and TUDCA on the vagotomy-induced damage of the biliary tree in the BDL rats. |
|In vitro||DMSO||20 mg/mL (26.15 mM)|
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