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SCC463
Sigma-AldrichsBT-RMS Spontaneous Brain-tropic RET Melanoma-sorted Mouse Cell Line
SCC463, the sBT-RMS spontaneous brain-tropic RET melanoma-sorted mouse cell line, demonstrates more aggressive brain metastasis than the parental RMS cell line, and exhibits higher organ specificity.
More>>SCC463, the sBT-RMS spontaneous brain-tropic RET melanoma-sorted mouse cell line, demonstrates more aggressive brain metastasis than the parental RMS cell line, and exhibits higher organ specificity. Less<<
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Übersicht
Replacement Information
Description
Catalogue Number
SCC463
Description
sBT-RMS Spontaneous Brain-tropic RET Melanoma-sorted Mouse Cell Line
Overview
SCC463 is a derivative of the SCC462 cell line. Parental SCC462 were isolated from a spontaneously occurring skin tumor in RET transgenic mice. The sBT-RMS cell line was isolated from the brain metastasis following the subdermal injection of RMS cells.5 sBT-RMS cells are more aggressive in brain metastasis than the parental RMS line and exhibited higher organ-specificity.
Alternate Names
sBT-RMS cell line
spontaneous brain tropic melanoma cell line
ret melanoma brain cell line
Background Information
The RET oncogene was originally created by an accidental in vivo recombination of two human genes, RET and RFP (the RET-finger protein, known today as TRIM27), during a transformation of NIH3T3 cells with human lymphoma DNA (Takahashi 1985). The founder RET transgenic mouse strains were generated by the embryonic microinjection of the RFP-RET oncogene under the mouse metallothionein-I promoter-enhancer (Iwamoto 1991), and a spontaneous metastatic melanoma model line was established by repetitive rounds of back-crossing of one of such founders (Kato 1998).
SOURCE: sBT-RMS cells are derived from the brain tumors that formed upon the subdermal injection of the Ret-melanoma sorted cells (RMS), which in turn were derived from the spontaneous metastatic skin tumors in the Ret-transgenic mice. The founder transgenic mice were created by microinjection of the Ret transgene into the fertilized egg of (C57BL/6 x BALB/c) x BALB/c mice.2 One of such founder mice was crossed with BCF1 (BALB/c x C57BL/6) mice to establish a transgenic line, designated “the 304 line.” When these F1 transgenic mice were subsequently crossed with C57BL/6 mice (coat color: black), BCF1 mice (agouti), and BALB/c mice (albino), benign melanocytic tumors often developed spontaneously in the pigmented F2 offspring but did not progress to metastatic tumors.2 The spontaneous metastatic melanoma model (designated the 304/B6 line), in which the parent of the RMS cells arose, was generated by 10 rounds of back-crossing of the 304 line with C57BL/6 mice.
REFERENCES 1. Takahashi M, Ritz J, Cooper GM. 1985. Activation of a novel human transforming gene, ret, by DNA rearrangement. Cell. 42(2): 581-588. 2. Iwamoto T, Takahashi M, Ito M, Hamatani K, Ohbayashi M, Wajjwalku W, Isobe K, Nakashima I. 1991. Aberrant melanogenesis and melanocytic tumour development in transgenic mice that carry a metallothionein/ret fusion gene. EMBO J. 10(11): 3167-3175. 3. Kato M, Takahashi M, Akhand AA, Liu W, Dai Y, Shimizu S, Iwamoto T, Suzuki H, Nakashima I. 1998. Transgenic mouse model for skin malignant melanoma. Oncogene. 17(14): 1885-1888. 4. Schwartz H, Blacher E, Amer M, Livneh N, Abramovitz L, Klein A, Ben-Shushan D, Soffer S, Blazquez R, Barrantes-Freer A, et al. 2016. Incipient melanoma brain metastases instigate astrogliosis and neuroinflammation. Cancer Res. 76(15):4359-4371. 5. Doron H, Amer M, Ershaid N, Blazquez R, Shani O, Lahav TG, Cohen N, Adler O, Hakim Z, Pozzi S, et al. 2019. Inflammatory activation of astrocytes facilitates melanoma brain tropism via the CXCL10-CXCR3 signaling axis. Cell Rep. 28(7): 1785-1798.
References
Product Information
Components
≥1x106 viable sBT-RMS cells: (Catalog No. SCC463). Store in liquid nitrogen.
SCC463, the sBT-RMS spontaneous brain-tropic RET melanoma-sorted mouse cell line, demonstrates more aggressive brain metastasis than the parental RMS cell line, and exhibits higher organ specificity.
Key Applications
Cell Culture
Application Notes
This product is intended for sale and sold solely to academic institutions for internal academic research use per the terms of the “Academic Use Agreement” as detailed in the product documentation. For information regarding any other use, please contact licensing@milliporesigma.com.
Biological Information
Host
Mouse
Cell Line Type
Cancer Cells
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Quality Assurance
• Each vial contains ≥1X10⁶ viable cells. • sBT-RMS cells are verified to be of mouse origin and negative for human, rat, Chinese hamster, Golden Syrian hamster, and non-human primate interspecies contamination, as assessed by a Contamination Clear panel by Charles River Animal Diagnostic Services • Cells tested negative for infectious diseases against a Mouse Essential CLEAR panel by Charles River Animal Diagnostic Services. • Cells tested negative for mycoplasma.
Usage Statement
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
This product contains genetically modified organisms (GMO). Within the EU GMOs are regulated by Directives 2001/18/EC and 2009/41/EC of the European Parliament and of the Council and their national implementation in the member States respectively. This legislation obliges Merck to request certain information about you and the establishment where the GMOs are being handled. Click here for Enduser Declaration (EUD) Form.
Storage and Shipping Information
Storage Conditions
sBT-RMS cells should be stored in liquid nitrogen until use. The cells can be cultured for at least 10 passages after initial thawing without significantly affecting the cell marker expression and functionality.