TTPA 抗体 (AA 82-108)
Quick Overview for TTPA 抗体 (AA 82-108) (ABIN1881957)
抗原
See all TTPA 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 82-108
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预测反应
- M, Rat
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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免疫原
- This TTPA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 82-108 amino acids from the Central region of human TTPA.
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亚型
- Ig Fraction
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应用备注
- WB: 1:1000
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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
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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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
- 4 °C,-20 °C
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有效期
- 6 months
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: "Rice endosperm iron biofortification by targeted and synergistic action of nicotianamine synthase and ferritin." in: Plant biotechnology journal, Vol. 7, Issue 7, pp. 631-44, (2009) (PubMed).
: "Association of variants in two vitamin e transport genes with circulating vitamin e concentrations and prostate cancer risk." in: Cancer research, Vol. 69, Issue 4, pp. 1429-38, (2009) (PubMed).
: "Isolated vitamin E deficiency mimicking distal hereditary motor neuropathy in a 13-year-old boy." in: Journal of child neurology, Vol. 23, Issue 11, pp. 1328-30, (2008) (PubMed).
: "Immunohistochemical localization of alpha-tocopherol transfer protein and lipoperoxidation products in human first-trimester and term placenta." in: European journal of obstetrics, gynecology, and reproductive biology, Vol. 140, Issue 2, pp. 183-91, (2008) (PubMed).
: "Ataxia with vitamin E deficiency associated with deafness." in: The Turkish journal of pediatrics, Vol. 50, Issue 5, pp. 471-5, (2008) (PubMed).
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: "Rice endosperm iron biofortification by targeted and synergistic action of nicotianamine synthase and ferritin." in: Plant biotechnology journal, Vol. 7, Issue 7, pp. 631-44, (2009) (PubMed).
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- TTPA (Tocopherol (Alpha) Transfer Protein (TTPA))
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别名
- TTPA
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背景
- This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa.
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分子量
- 31750
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NCBI登录号
- NP_000361
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UniProt
- P49638
抗原
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