- ￥4000
- GeneTex
- 美国
- GTX00416-pro
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, store at -20ºC or below. After reconstitution, keep as concentrated solution. Avoid freeze-thaw cycles.
- 保质期：
12 months from the shipping date of the product.
- 英文名：
Human C5a protein, His and Fc tag (active)
- 库存：
Available
- 供应商：
GeneTex
- 规格：
10 μg
The chemotactic effect of GTX00416-pro Human C5a protein (active).
Upper: (A)THP-1 cells were seeded into the upper chambers and serum free RPMI-1640 without C5a was added in lower chamber, then cells in lower chamber were observed at low magnification (×100) after incubation for 3hrs.
(B) THP-1 cells were seeded into the upper chambers and 50 ng/ml C5a was added in lower chamber, then cells in lower chamber were observed at low magnification (×100) after incubation for 3hrs.
(C) THP-1 cells were seeded into the upper chambers and 100 ng/ml C5a was added in lower chamber, then cells in lower chamber were observed at low magnification (×100) after incubation for 3hrs.
Lower: The number of migrated cells were counted at high magnification (×400) randomly (five fields for each filter).
WB analysis of GTX00416-pro Human C5a protein (active).
SDS-PAGE analysis of GTX00416-pro Human C5a protein (active).
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文献和实验Purification of Human Multiprotein Complexes using OneSTrEP Technology
sufficient for visualising single protein bands by Coomassie Blue staining (Figure 1). The Strep -tag®II (SAWRHPQFGG) and its “double” sister, the One-STrEP-tag (tandem arrangement of Strep -tag®II, here called OneStrep), are reasonably small protein
Chromatin Interaction Analysis Using Paired‐End Tag Sequencing
Analysis using Paired?End Tag sequencing (ChIA?PET) is a technique developed for large?scale, de novo analysis of higher?order chromatin structures. Cells are treated with formaldehyde to cross?link chromatin interactions, DNA segments bound by protein
Identifying Protein Interactions by Hydroxyl‐Radical Protein Footprinting
Basic Protocol 1: Generation of an Active Recombinant Protein That is End‐Labeled Basic Protocol 2: Hydroxyl Radical Cleavage of Protein in Absence and Presence of Ligand Basic Protocol 3: Analyze Gel
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