- ￥1800
- GeneTex
- 美国
- GTX50875
- 2025年07月14日
- WB
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- 详细信息
- 文献和实验
- 技术资料
- 形态：
Liquid
- 保存条件：
Store at 4ºC short term (3 months). For extended storage aliquot and store at -20ºC or below. Avoid freeze-thaw cycles.
- 保质期：
12 months from the shipping date of the product.
- 目录编号：
GTX50875
- 级别：
Reagents
- 库存：
Available
- 供应商：
GeneTex
- 应用范围：
WB
- 抗体英文名：
Trident Prestained Protein Ladder (High Range)
- 抗体名：
Trident Prestained Protein Ladder (High Range)
- 规格：
500 μl
Migration pattern of GTX50875 Trident Prestained Protein Ladder (High Range) in Tris-Glycine gel.
Migration pattern of GTX50875 Trident Prestained Protein Ladder (High Range) in Bis-Tris- gel.
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文献和实验M?rquez-Valadez B et al., Front Neurosci 2019 (PMID:31040765)
Berenice M?rquez-Valadez et al., Front. Neurosci. 2019 (Epub)
Khandelwal S et al., Int J Mol Sci 2018 (PMID:30373175)
Santos MF et al., J Biol Chem 2018 (PMID:30018135)
Rappa G et al., Oncotarget 2015 (PMID:25762645)
Rappa G et al., Mol Cancer Res 2014 (PMID:25103498)
Zhang DY et al., ACS Chem Neurosci 2022 (PMID:35713284)
S Park et al., J Bacteriol 2023 (PMID:37199658)
Santos MF et al., Cells 2022 (PMID:36010551)
Santos MF et al., J Extracell Vesicles 2021 (PMID:34429859)
Shubin CB et al., Elife 2020 (PMID:32597753)
Valle-Bautista R et al., Front Cell Dev Biol 2020 (PMID:33042999)
into the wells of the SDS-PAGE gel. Load an appropriate amount of Trident Blue Prestained Protein Ladder or Trident Prestained Protein Ladder to one or more additional lanes.2. Run the gel in 1X Trident Running Buffer for 1-2 hours at 50-100 V.We recommend
Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
that bridge distant genomic regions, while simultaneously identifying such physical proximities. This method is also useful for determining if a candidate protein might mediate long-range interactions, both in cis and in trans in the nucleus. We discuss
HIGH RESOLUTION GENETIC FOOTPRINTING
This web site was designed to provide detailed protocols for genetic footprinting, a technique for high-resolution mapping of the functional organization of cloned genes (Singh, Crowley and Brown (1997) PNAS 94: 1304-1309
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