Recombinant PEX11B 抗体
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北京 101111
Quick Overview for Recombinant PEX11B 抗体 (ABIN7881918)
抗原
See all PEX11B 抗体抗体类型
适用
宿主
克隆类型
标记
应用范围
克隆位点
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原理
- PEX11B Antibody / Peroxisomal membrane protein 11B
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纯化方法
- Affinity-chromatography
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免疫原
- A synthesized peptide derived from human PEX11B was used as the immunogen for the PEX11B antibody.
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亚型
- IgG
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应用备注
- Optimal dilution of the PEX11B antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Rabbit IgG in phosphate buffered saline, pH 7.4, 150 mM NaCl, 0.02 % sodium azide and 50 % glycerol, 0.4-0.5 mg/mL BSA
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store the PEX11B antibody at -20oC.
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- PEX11B (Peroxisomal Biogenesis Factor 11 beta (PEX11B))
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别名
- PEX11B
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背景
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PEX11B antibody detects PEX11B, a peroxisomal biogenesis factor encoded by the PEX11B gene. Other names include peroxisomal membrane protein 11B and PMP11B. PEX11B is a peroxisomal membrane protein that regulates peroxisome proliferation and division. It belongs to the PEX11 family, which control peroxisome number and morphology. PEX11B promotes peroxisomal elongation, constriction, and fission, ensuring proper distribution of peroxisomes during cell division and differentiation. Peroxisomes are essential organelles involved in lipid metabolism, reactive oxygen species detoxification, and bile acid synthesis, making PEX11B critical for cellular homeostasis.
PEX11B antibody is widely applied in cell biology, metabolism, and disease research. By detecting PEX11B, researchers can explore how peroxisomes multiply and adapt to metabolic demands. Knockout studies show that PEX11B deficiency leads to reduced peroxisome number, altered lipid metabolism, and developmental abnormalities. This highlights its importance in peroxisome biogenesis disorders.
Applications include western blotting, immunohistochemistry, immunofluorescence, and ELISA. Western blotting identifies PEX11B protein in peroxisome enriched fractions, immunohistochemistry maps tissue distribution in liver and kidney, and immunofluorescence highlights peroxisomal membranes. These assays provide robust tools for evaluating peroxisome biology in health and disease.
Mutations in PEX11B cause peroxisome biogenesis disorders characterized by cataracts, intellectual disability, and developmental delay. These disorders illustrate the essential role of PEX11B in organelle maintenance. By applying PEX11B antibody, scientists can investigate peroxisomal dynamics, inheritance, and disease mechanisms. In addition, altered peroxisome function is linked to metabolic syndromes, cancer, and neurodegeneration, making PEX11B relevant beyond rare genetic disease.
PEX11B interacts with dynamin like proteins and other peroxisome fission factors, coordinating peroxisome proliferation with mitochondrial dynamics. This crosstalk underscores its importance in cellular energy balance. NSJ Bioreagents provides PEX11B antibody with strong specificity, supporting accurate detection of this essential peroxisomal protein in both basic and translational studies. -
UniProt
- O96011
抗原
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