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SC-10

SC-10 is a chemical compound with the molecular formula C₁₀H₁₆.
It is a volatile organic compound that is commonly used as a solvent and as a precursor in the production of various chemical products.
SC-10 has a pungent odor and is flammable, requiring caution during handling and storage.
This substance is of interest in industrial and research applications due to its unique chemical properties and potential uses.
However, further study is needed to fully understand its safety profile and environmental impact.

Most cited protocols related to «SC-10»

For analysis of LFP signals, a total of 35 mice were used, 13 for the EE-OLD group, 10 for the SC-OLD group, 6 for the EE-YOUNG group and 6 for the SC-YOUNG group. For comparing the results of Fourier analysis (Figure 3 and Figure S1), Three-Way ANOVA followed by Holm-Sidak post-hoc test was used, with factors “rearing” (with levels EE and SC), “age” (with levels AGED and YOUNG) and “cortical area” (with levels A1 and V1). For comparing the results of Cross correlation analysis (Figure 4 and Figure S2), Two-Way ANOVA followed by Holm-Sidak post-hoc test was used.
For Western blots on vGluT-1 and vGAT (Figure 5), a total of 26 mice were used, 12 for the EE-OLD group, 9 for SC-OLD group and 5 for the SC-YOUNG group. Statistical significance was assessed using One-Way ANOVA followed by Tukey post-hoc test.
For Western blots on amyoid-β oligomers and neprilysin (Figures 6, 7), a total of 36 mice were used, 22 for the EE-OLD group and 14 for the SC-OLD group. Statistical significance was assessed using Student's t-test.
All the analyses have been performed using the SigmaPlot 12 software (SyStat Software, USA).
Data are presented as mean ± s.e.m.
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Publication 2013
Cortex, Cerebral Mice, House Neprilysin neuro-oncological ventral antigen 2, human SC-10 Western Blot
As described in our previous studies [29 (link)], lentiviral particles containing the p53-shRNA-1 (Santa Cruz, sc-29435-V), p53 shRNA-2 (Genechem, Shanghai, China) or AMPKα1 shRNA (Santa Cruz, sc-29673-V) (10 μL/well) were added to cultured CRC cells for 24 h. Afterwards, cell culture medium was replaced with puromycin (0.5 μg/mL)-containing complete medium. The medium was renewed every 2-3 days until resistant stable colonies were formed. Expression of targeted protein (AMPKα1 and p53) was always determined by Western-blots in resulting stable cells. Same amount of scramble control shRNA lentiviral particles (Santa Cruz, sc-108080) were added to control cells.
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Publication 2016
Cell Culture Techniques Cells Cultured Cells Puromycin SC-10 Short Hairpin RNA Western Blot

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Publication 2022
Arabidopsis Cells Chloroplasts Chromium Cytosol Gene Annotation Gene Expression Genes Genes, Mitochondrial Genome Mitochondrial Inheritance Oryza sativa Plant Roots Rice SC-10
A total of 271 in-hospital patients with non-malignant pain were recruited over an eight-month period, among which 30 patients were exclusively used for testing the pre-final version of SC-PCS; 37 patients were removed due to exclusionary criteria and 4 due to floor and ceiling effects. The remaining 200 patients were used in all analysis presented. The inclusion criteria were as follows: (1) age over 18 years, (2) ability to read and write SC and accurately understand SC-PCS and other questionnaires, and (3) pain duration greater than 12 weeks. Exclusion included tumor, inability to comprehend instructions or lack of consent for study participation. All study procedures were approved by the Institutional Review Board of the Second Affiliated Hospital and Yuying’s Children Hospital, Wenzhou Medical University.
The minimum number of participants for evaluating factor analysis and internal consistency, for assessing concurrent validity, and for testing temporal reliability is 100, 52, and 30, respectively.42 (link),43 We anticipated to recruit 150, 75, and 30 patients who would complete SC-PCS, SC-PCS with five other questionnaires, and additional SC-PCS 10 days after the initial query, respectively. Since participants were recruited from a hospital setting, the first two numbers were easily exceeded (N = 200 and 81). However, because most patients were hospitalized for less than one week, the number of patients for assessing temporal reliability was slightly below the anticipation (N = 24).
All patients completed a battery of questionnaires including a 10-item demographic survey regarding age, gender, residence (urban/rural), marriage, education, and employment status as well as pain VAS, pain duration, and the SC-PCS. Eighty-one patients were chosen to complete five additional five questionnaires (BDI, PANAS, PASS, PSQ, and ODI) in order to construct an internal validity of the SC-PCS. A total of 24 patients were chosen to complete the SC-PCS a second time 10 days after the initial completion to assess temporal stability. In order to minimize pain influence in the temporal stability analysis, only patients whose pain VAS remained invariant over a 10-day period completed a second SC-PCS. All questionnaires were collected on an electronic tablet device and were collected using Research Electronic Data Capture (REDCap).44 (link) REDCap is a secure, convenient, and efficient online/offline web application for capturing electronic survey data and is recommended by the National Institutes of Health for data collection in clinical trials.
Publication 2018
Ethics Committees, Research Gender Inpatient Medical Devices Neoplasms Pain Patients SC-10 Tablet Visual Analog Pain Scale
Three separate teams conducted the study to reduce any potential bias in data collection (Stellenbosch), intervention implementation (the Philani Program), and analyses (UCLA). From May 2009 to September 2010, the Stellenbosch team hired local township mothers to recruit pregnant women who were at least 18 years old, living within the target neighbourhood, and able to give informed consent. Each recruiter worked in one PIP and one SC neighbourhood to ensure that recruiter competence was similar across conditions. Pregnant women were recruited at an average 26 weeks of pregnancy (range, 3–40 weeks); only 2% of women refused participation. Initially, however, we identified 22% fewer pregnant women in SC. By redeploying recruiters, we identified an additional 94 women in 10 of the 12 SC neighbourhoods who were pregnant during the recruitment period (median of 7 late-entry participants per neighbourhood; range, 3–24). These women were enrolled post-birth when their infants were a mean age of 9 months old (range, 1–18 months). The final sample (n=1238) comprised a median of 51 pregnant women per neighbourhood (range, 23–72).
Figure 1 summarizes participant flow from recruitment to six months post-birth. Follow-up rates were similar across intervention conditions: 92% were reassessed post-birth (M=1.9 weeks; SD=2.1), 88% at six months (M=6.2 months, SD=0.7), and 88% were assessed at all three points. Due to delayed enrolment, late-entry participants were asked baseline, post-birth and 6-month questions in one assessment.
Publication 2013
AN 12 Childbirth Infant Mothers Pregnancy Pregnant Women SC-10 Woman

Most recents protocols related to «SC-10»

Chromatin immunoprecipitation (ChIP) assays were performed essentially as described before (Dong et al, 2022 (link)). In brief, chromatin in control and treated cells were cross‐linked with 1% formaldehyde. Cells were incubated in lysis buffer (150 mM NaCl, 25 mM Tris pH 7.5, 1% Triton X‐100, 0.1% SDS, 0.5% deoxycholate) supplemented with protease inhibitor tablet and PMSF. DNA was fragmented into ~200 bp pieces using a Branson 250 sonicator. Aliquots of lysates containing 200 μg of protein were used for each immunoprecipitation reaction with 5 μg of anti‐BRG1 (Santa Cruz, cat# sc‐10,768), anti‐E2F1 (Cell Signaling Tech, cat# 3472), or pre‐immune IgG.
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Publication 2023
Biological Assay Buffers Cells Chromatin Deoxycholate E2F1 protein, human Formaldehyde Immunoprecipitation Immunoprecipitation, Chromatin Protease Inhibitors Proteins SC-10 SMARCA4 protein, human Sodium Chloride Tablet Triton X-100 Tromethamine
Whole cell lysates were obtained by re‐suspending cell pellets in RIPA buffer (50 mM Tris pH7.4, 150 mM NaCl, 1% Triton X‐100) with freshly added protease inhibitor (Roche). Western blot analyses were performed with anti‐BRG1 (Santa Cruz, cat# sc‐10,768, 1:1000) and anti‐β‐actin (Sigma, cat# A2228, 1:5000) antibodies.
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Publication 2023
Actins Antibodies Buffers Cells Pellets, Drug Protease Inhibitors Radioimmunoprecipitation Assay SC-10 SMARCA4 protein, human Sodium Chloride Triton X-100 Tromethamine Western Blot
The whole part of AM plant was gathered from the semi-arid rangeland of Torbat-e Jam in July 2021. This area is 8184 square kilometers, from 60° 15´E to 60° 30´E, and 34° 35´N to 35° 47´N. In average, its height is 928 m above sea level. The samples were chapped with a laboratory chopper into pieces of about 2 cm. The chapped samples were ensiled in a 3.5 kg polyethylene mini-silos for 60 days. Fresh AM was ensiled in the mini-silos (3.5 kg) and treated with 1] no additive (control, AM1), 2] 5% molasses (AM2), 3] 10% molasses (AM3), 4] 1 × 104 CFU (colony forming units)/g of fresh silage (AM4), 5] 1 × 104 CFU of SC/g of fresh silage + 5% molasses (AM5), 6] 1 × 104 CFU of SC/g of fresh silage + 10% molasses (AM6), 7] 1 × 108 CFU of SC/g of fresh silage (AM7), 8] 1 × 108 CFU of SC/g of fresh silage + 5% molasses (AM8), 9] 1 × 108 CFU of SC/g of fresh silage + 10% molasses (AM9) for 60 days. Five replicates were considered for each treatment. Kimiazyme Company (Tehran, Iran) prepared the SC (8 × 1010 CFU/g of fresh material) with the trade name Zy-MOS Ultra.
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Publication 2023
Molasses Plants Polyethylene, High-Density SC-10 Silage
The original RS-SC is a 25-item resilience instrument specific to cancer that has five domains of generic element, benefit finding, support and coping, hope for the future, and meaning for existence (19 (link), 20 (link)). RS-SC is rated based on a five-point Likert scale, with higher scores indicating higher resilience levels (score ranges from 25 to 125). In this study, a short-form of 10-item RS-SC (RS-SC-10) was administered (21 (link)–23 (link)). RS-SC and RS-SC-10 were attached in the Supplementary material.
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Publication 2023
Generic Drugs Malignant Neoplasms SC-10

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Publication 2023
Alamar Blue Antagomirs Biological Assay Cell Culture Techniques Cells Cell Survival Culture Media Fluorescence inhibitors Lipids Liposomes MicroRNAs SC-10 Serum Signal Transduction TGF-beta1

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The Sc-10 is a laboratory instrument designed for the preparation and analysis of biological samples. It is a core piece of equipment used in various life science research applications.
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Anti-Met (sc-10) is a mouse monoclonal antibody that recognizes the Met receptor tyrosine kinase. The antibody is designed for use in western blotting, immunoprecipitation, and immunohistochemical applications.
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The BD LSR II flow cytometer is a laboratory instrument designed to analyze and sort cells or particles in a fluid sample. It utilizes laser technology to detect and measure various properties of the cells or particles, providing data on their size, granularity, and fluorescent characteristics.
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Mouse serum is a biological fluid derived from the blood of laboratory mice. It contains a variety of proteins, hormones, and other biomolecules that are naturally present in the mouse circulatory system.
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The GAPDH antibody is a primary antibody that recognizes the GAPDH (Glyceraldehyde 3-phosphate dehydrogenase) protein. GAPDH is a key enzyme involved in the glycolytic pathway and is commonly used as a loading control or housekeeping gene in various research applications.
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Immobilon-P PVDF membrane is a polyvinylidene difluoride (PVDF) membrane designed for protein transfer and immobilization in Western blotting and other protein analysis applications. The membrane provides high protein-binding capacity and is compatible with a variety of detection methods.
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EGF is a laboratory equipment product manufactured by Merck Group. It is a protein that plays a key role in cell growth and differentiation processes. EGF primarily functions as a growth factor, stimulating cell division and proliferation in various cell types.
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Puromycin is a laboratory product manufactured by Merck Group. It functions as an antibiotic that inhibits protein synthesis in eukaryotic cells.
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The Anti-AKT product is a primary antibody that specifically binds to the AKT protein. AKT is a serine/threonine kinase that plays a crucial role in various cellular processes, such as cell growth, proliferation, and survival. The Anti-AKT antibody can be used for the detection and analysis of AKT in various experimental applications, including Western blotting, immunoprecipitation, and immunohistochemistry.
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The RNeasy Mini Kit is a laboratory equipment designed for the purification of total RNA from a variety of sample types, including animal cells, tissues, and other biological materials. The kit utilizes a silica-based membrane technology to selectively bind and isolate RNA molecules, allowing for efficient extraction and recovery of high-quality RNA.

More about "SC-10"

SC-10 is a volatile organic compound (VOC) with the chemical formula C₁₀H₁₆.
It is commonly used as a solvent and as a precursor in the production of various industrial and research products.
SC-10, also known as Anti-Met (sc-10), is a substance of interest due to its unique properties and potential applications.
The BD LSR II flow cytometer is a popular instrument used in research applications involving SC-10 and related compounds.
Mouse serum and GAPDH antibody are often used in conjunction with SC-10 for various analytical procedures.
In addition, Immobilon-P PVDF membrane, EGF, Puromycin, and Anti-AKT are some other related terms and products that may be encountered in research involving SC-10.
The RNeasy Mini Kit is a commonly used tool for RNA extraction and purification, which can be relevant in studies examining the effects of SC-10 or related substances.
While SC-10 has many industrial and research applications, further stdudy is needed to fully understand its safety profile and environmental impact.
Researchers and industry professionals must exercise caution when handling and storing this flammable and pungent-smelling compound.