A23187 (Calcimycin)

貨號 Cat. No.
A-600
規格 Size
10x1mg 5mg 5x5mg

Description

A23187 (Calcimycin)


Widely Used Ca2+ Ionophore











Product#: A-600

























Sizes:
10 x 1 mg
5 mg
5 x 5 mg
 
 
 














M.W.: 523.6 daltons










CAS No.:

[52665-69-7]














Structure:
.








 












Bioassay:
The biological activity was tested to confirm the ability of A23187 to induce apoptosis in Jurkat cells.

 













Jurkat cells were grown to 70% confluency. A23187 (2 mM) or vehicle were added to cell culture for 6 hours.

At the end of the incubation, the cells were extracted and blotted.

Apoptosis was probed by detection of cleaved Caspase 3 using Caspase 3 specific antibodies.









 









References:


















































1.



Berridge, M.J. (1993) Nature 361, 315.



2.


Scharff, O. et al. (1993) Physiol. Rev. 73, 547.

3.


Orrenius, S. et al. (2003) Nat. Rev. Mol. Cell Biol. 4, 552.

4.


Hajnoczky, G. et al. (2003) Biochem. Biophys. Res. Commun. 304, 445.

5.


Caron-Leslie, L.A. et al. (1991) Mol. Endocrinol. 5, 1169.

6.


Caron-Leslie, L.A. et al. (1994) FASEB J. 8, 639.

7.


Rzigalinski, B.A. et al. (1994) Biochim. Biophys. Acta 1223, 219.

8.


Vrana, J.A. et al. (1998) Int. J. Oncol. 12, 927.

9.


Petersen, A. et al. (2000) Brain Res. 857, 20.

10.


Cheng, C.H. et al. (2002) FEBS Lett. 516, 191.

11.



Jansen, S. et al. (2003) Biol. Trace Elem. Res. 96, 133.




A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusensis. It is used to increase intracellular Ca2+ levels, and for in vitro studies related to intracellular Ca2+ mediated events. A23187 can cause cell activation, differentiation, or proliferation and thus mimics cellular processes observed in response to cytokines and growth factors.1,2

Furthermore, A23187 induces in a concentration and time-dependent manner, Ca2+ triggered cell apoptosis.3,4 This property was exploited to clarify apoptotic events in different cell lines such as mouse lymphoma cell line (S49),5,6 histiocytic lymphoma U937,7 human myeloid leukemia cells (HL-60),8 cultured striatal neurons,9 renal tubular cells,10 and C6 glioma cells.11


 


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