Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
A potent synthetic anti-estrogenic agent. A cell-permeable and reversible inhibitor of protein kinase C (IC50 = 10 µM). Induces apoptosis in human malignant glioma cell lines and inhibits prostate cancer cell growth by induction of p21 protein.
Catalogue Number
579000
Brand Family
Calbiochem®
Synonyms
Estrogen Receptor Signaling Regulator I
References
References
Rohlff, C., et al. 1998. Prostate 37, 51. Couldwell, W.J., et al. 1994. FEBS Lett.345, 43. Baltuch, G.H., et al. 1993. Neurosurgery33, 495. Powis, G. 1991. Trends Pharmacol. Sci.12, 188. Issandou, M., et al. 1990. Cancer Res.50, 5845. O’Brian, C.A., et al. 1985. Cancer Res.45, 2462.
Harmful if swallowed. May cause cancer. May impair fertility. May cause harm to the unborn child. May cause harm to breastfed babies.
S Phrase
S: 36/37/39-45
Wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
Product Usage Statements
Storage and Shipping Information
Ship Code
Ambient Temperature Only
Toxicity
Harmful & Carcinogenic / Teratogenic
Storage
+2°C to +8°C
Do not freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
产品目录编号
GTIN
579000-100MGCN
04055977265934
Documentation
Tamoxifen Citrate - CAS 54965-24-1 - Calbiochem MSDS
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
11-January-2010 RFH
Synonyms
Estrogen Receptor Signaling Regulator I
Description
A potent synthetic anti-estrogen. A cell-permeable and reversible inhibitor of protein kinase C (IC50 = 10 µM). Induces apoptosis in human malignant glioma cell lines.
Form
White to off-white powder
CAS number
54965-24-1
RTECS
KH2387000
Chemical formula
C₂₆H₂₉NO · C₆H₈O₇
Structure formula
Purity
≥99% by HPLC
Solubility
Ethanol (5 mg/ml), Methanol (5 mg/ml), or sparingly soluble in H₂O
Storage
+2°C to +8°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity
Harmful & Carcinogenic / Teratogenic
Merck USA index
14, 9048
References
Rohlff, C., et al. 1998. Prostate 37, 51. Couldwell, W.J., et al. 1994. FEBS Lett.345, 43. Baltuch, G.H., et al. 1993. Neurosurgery33, 495. Powis, G. 1991. Trends Pharmacol. Sci.12, 188. Issandou, M., et al. 1990. Cancer Res.50, 5845. O’Brian, C.A., et al. 1985. Cancer Res.45, 2462.