- ￥7956
- Biorbyt
- orb413405
- 英国
- 2026年07月24日
- ELISA, WB
- Mouse
- All
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- 文献和实验
- 技术资料
- 抗体名：
4-Hydroxy-2-hexenal Antibody 抗体
- 抗体英文名：
4-Hydroxy-2-hexenal Antibody
- 靶点：
4-Hydroxy-2-hexenal
- 浓度：
1 mg/ml
- 应用范围：
ELISA, WB
- 宿主：
Mouse
- 适应物种：
All
- 保质期：
12 months from date of receipt.
- 抗原来源：
详询
- 目录编号：
orb413405
- 级别：
科研
- 库存：
99
- 供应商：
Biorbyt
- 标记物：
Unconjugated
- 克隆性：
Monoclonal
- 保存条件：
详询
- 亚型：
IgG1
- 免疫原：
详询
- 规格：
100 ug
描述: Mouse monoclonal antibody to 4-Hydroxy-2-hexenal
克隆号: 5C11.1
别名: 4-Hydroxy-2-hexenal, 4-Hydroxyhex-2-enal, 4-Hydroxyhexenal, 4-Hydroxy Hexenal, Hex-2-enal, 4-hydroxy-, Hexenal, 4-hydroxy-, 2-Hexenal, 4-hydroxy-, (E)-, (2E)-4-Hydroxy-2-hexenal, (E)-4-Hydroxy-2-hexenal
应用稀释比例: WB (1:1000); ELISA (1:1000)
应用说明: A 1:1000 dilution was sufficient for detection of 4-Hydroxy-2-hexenal in 1 µg of 4-Hydroxy-2-hexenal-BSA conjugate by ECL immunoblot analysis using goat anti-mouse IgG:HRP as the secondary antibody.
免疫原: Synthetic 4-Hydroxy-2-hexenal modified Keyhole Limpet Hemocyanin (KLH)
防腐剂: PBS pH 7.4, 50% glycerol, 0.09% sodium azide. Storage buffer changes when conjugated.
纯化方法: Protein G Purified
特异性: Specific for 4-Hydroxy-2-hexenal. Slight cross-reactivity with 4-Hydroxynonenal. Does not cross-react with Acrolein, Crotonaldehyde, Hexanoyl Lysine, Malondialdehyde, or Methylglyoxal modified proteins.
研究领域: Cancer Biology, Cell Biology, Metabolism Research
保存条件: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
备注: For research use only.
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文献和实验4-Hydroxy-2-Nonenal (4-HNE) Staining by Anti-HNE Antibody
using an anti-4-HNE monoclonal antibody (MAb) (6 –8 ) and labeled goat anti-mouse IgG antibody (9 ).
to mutagenesis, carcinogenesis, degenerative diseases, cancer, diabetes, and aging ( 1 – 16 ). With this in mind, the DNA nucleoside 2′-deoxyguanosine (dG) undergoes a hydroxylation reaction at the C-8 position to yield a useful biomarker, 8-hydroxy-2′
) and 4-hydroxy-2-nonenal (HNE) (3 ), a major product of lipid peroxidation and the most reactive of these compounds under physiological conditions (4 ). This fluorescent compound, characterized as a2-hydroxy-3-imino-1,2-dihydropyrrol derivative (3, R1 = R2
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