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1801

Sigma-Aldrich

α-Naphthyl Butyrate Solution

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About This Item

UNSPSC Code:
41116124
NACRES:
NA.47

form

solution

Quality Level

IVD

for in vitro diagnostic use

concentration

2.4 g/L

application(s)

hematology
histology

shipped in

dry ice

storage temp.

−20°C

Application

Intended for use in the Sigma α-Butyrate Esterase kit, procedure 181B

Packaging

2.4g/L alpha-naphthyl butyrate in methanol solution with stabilizers

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3 - STOT SE 1

Target Organs

Eyes,Central nervous system

WGK

WGK 3


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Michael D'Angelica et al.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 24(9), 1221-1228 (2011-05-17)
Folate receptor alpha (FRα), encoded by folate receptor 1 (adult) gene, has emerged as a cancer biomarker and potential therapeutic target. In addition, its expression in tumors may offer prognostic information. The aim of this study was to assess the
N F Li et al.
Cell proliferation, 40(5), 780-794 (2007-09-20)
Cell immortalization is considered to be a prerequisite status for carcinogenesis. Normal human ovarian surface epithelial (OSE) cells, which are thought to be the origin of most of human ovarian carcinomas, have a very limited lifespan in culture. Establishment of
A Kaida et al.
Oncogene, 19(6), 827-830 (2000-03-04)
We have previously demonstrated that the human T-cell leukemia virus type 1 (HTLV-1) Tax oncoprotein represses the trans-activation function of p53 tumor suppressor protein. Recently, several proteins with sequence homology to p53 have been identified. In this study, we demonstrated
Sara Cattelani et al.
Neoplasia (New York, N.Y.), 14(7), 634-643 (2012-08-21)
The p53 gene is rarely mutated in neuroblastoma, but codon 72 polymorphism that modulates its proapoptotic activity might influence cancer risk and clinical outcome. We investigated whether this polymorphism affects neuroblastoma risk and disease outcome and assessed the biologic effects
Y Ariumi et al.
Oncogene, 19(12), 1491-1499 (2000-03-29)
The human T-cell leukemia virus type 1 (HTLV-1) Tax oncoprotein repressed the transcriptional activity of wild-type p53 through its N-terminal trans-activation domain. Although Tax did not directly bind to p53, this repression required the activation of CREB pathway by Tax.

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