9(S)-HOTrE
Based on 1 Customer Validation
9(S)-HOTrE is a PPARα activator and an inducer of apolipoprotein A-I (apoA-I) mRNA expression. 9(S)-HOTrE upregulates the expression of PPARα target gene CPT1α. 9(S)-HOTrE can be used in the research of cardiovascular diseases.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- Purity : 99.9%
- CAS No.: 89886-42-0
- 화학식: C18H30O3
- 분자량:294.43
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보관:
Solution, -20°C, 2 years
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
- Protocol
- 순도&문서
- References
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Help & FAQs
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Biological Activity
제품 설명
IC50 & Target
[1]|
CPT-1A |
PPARα |
In Vitro
9(S)-HOTrE (9 μg/mL; 16 h) potently activates the transcriptional activity of PPARα in HEK293 cells, and its activity at the concentration of 9 μg/mL is 11.6 times higher than that of the control group[1].
9(S)-HOTrE (10 μg/mL) activates PPARα in HepG2 cells, and at the concentration of 10 μg/mL, it increases the expression level of CPT1α mRNA by 8.0-fold compared with the control group[1].
9(S)-HOTrE (0.01-10 μg/mL) regulates the expression level of apoA-I mRNA in HepG2 cells[1].
9(S)-HOTrE (0.01-0.1 μg/mL) upregulates KEAP1 mRNA expression in HepG2 cells at concentrations that stimulate apoA-I transcription (0.01 μg/mL and 0.05 μg/mL), while it downregulates KEAP1 mRNA expression at the concentration of 0.1 μg/mL[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
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Cell Line:HepG2 cells
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Concentration:0.01, 0.05, 0.1, 0.5, 1, 3, 5, 7, 8.3, 10 μg/mL
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Incubation Time:/
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Result:Increased apoA-I mRNA expression by 35% in HepG2 cells at an optimal concentration of 0.05 μg/mL, while reduced apoA-I mRNA expression at higher concentrations (≥3 μg/mL).
Chemical Information
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CAS No. 89886-42-0
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Appearance Liquid
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분자량 294.43
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화학식 C18H30O3
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Color Colorless to light yellow
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SMILES
CC/C=C\C/C=C\C=C\[C@@H](O)CCCCCCCC(O)=O
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Structure Classification
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Initial Source
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Solution, -20°C, 2 years
Protocol
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RT-PCR
Reverse transcription technology uses RNA as a template to synthesize DNA. RT-PCR is simple, specific and sensitive, and can be used to detect gene expression levels and expression differences in cells; detect RNA virus content; clone cDNA sequences of specific genes.
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RNA extraction experimental
By lysing cells, releasing RNA, and removing impurities such as proteins and DNA, high-purity RNA products are finally obtained. The commonly used traditional method is the guanidine isothiocyanate/phenol/chloroform method (Trizol), which is suitable for a variety of animal materials including animal tissues, microorganisms, cultured cells, etc., and most plant materials.
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Real Time qPCR (Q-PCR)
Real-time quantitative PCR (qPCR) quantifies an amplifiable nucleic-acid target by monitoring fluorescence during PCR cycling rather than measuring product only after amplification. The increase in fluorescence tracks accumulation of PCR product, and the quantification cycle (Cq; historically also Ct/CP) is related to the initial amount of target: samples containing more starting target generally reach the defined fluorescence threshold in fewer cycles.
순도&문서
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Data Sheet (265 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
9(S)-HOTrE Related Classifications
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