- 询价
- Agrisera
- Sweden
- AS20 4510-1ml
- 2025年10月05日
- ELISA (ELISA), Immunocytochemistry (ICC), Immunoflourescence (IF), Western blot (WB)
- Mouse
- Arabidopsis thaliana
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
MAP- conjugated peptide of Arabidopsis thaliana ARP8, C-terminal UniProt: Q9FKT0-1, TAIR: At5g56180
- 亚型：
IgG1
- 形态：
Cell culture supernatant
- 保存条件：
Store at -20°C; Avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.
- 克隆性：
Monoclonal
- 适应物种：
Arabidopsis thaliana
- 供应商：
Agrisera
- 宿主：
Mouse
- 应用范围：
ELISA (ELISA), Immunocytochemistry (ICC), Immunoflourescence (IF), Western blot (WB)
- 靶点：
Anti-ARP8 | Actin-related protein 8, (clone 12F5,D4,C3), C-Terminal
- 抗体英文名：
Anti-ARP8 | Actin-related protein 8, (clone 12F5,D4,C3), C-Terminal
- 抗体名：
Anti-ARP8 | Actin-related protein 8, (clone 12F5,D4,C3), C-Terminal
- 规格：
1 ml
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文献和实验Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
between chromatin elements without specifically identifying the protein components that mediate such interactions. Here we describe a detailed protocol for C ombined 3C -C hIP-C loning (6C) technology, which combines multiple techniques to identify the proteins
Combine actin + GST-fusion protein and incubate for 1 hr. x 4¡C. Add 20ul 50% glutathione agarose equilibrated into binding buffer. Incubate 15 min x 4¡C with frequent mixing. Wash beads 4 times with binding buffer, spin down 4-8000 rpm
buffer. Combine actin + GST-fusion protein and incubate for 1 hr. x 4¡C. Add 20ul 50% glutathione agarose equilibrated into binding buffer. Incubate 15 min x 4¡C with frequent mixing. Wash beads 4 times with binding
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