PEX1 抗体 (Middle Region)
Quick Overview for PEX1 抗体 (Middle Region) (ABIN954094)
抗原
See all PEX1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 606-637, Middle Region
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特异性
- This antibody recognizes Human Peroxin 1 / PEX1 (Center).
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纯化方法
- Protein A column, followed by peptide affinity purification
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免疫原
- KLH conjugated synthetic peptide between 606-637 amino acids from the Central region of Human Peroxin 1 / PEX1
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亚型
- Ig Fraction
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anti-Peroxisomal Biogenesis Factor 1 (PEX1) (AA 927-1283) antibody
PEX1 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 1 (PEX1) (AA 62-219) antibodyPEX1 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 1 (PEX1) (AA 172-377) antibodyPEX1 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 1 (PEX1) (AA 63-157) antibodyPEX1 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 1 (PEX1) (Internal Region) antibodyVerified PEX1 适用: 小鼠, 大鼠 ELISA, WB 宿主: 山羊 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 1 (PEX1) (AA 1-1283) antibodyPEX1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 1 (PEX1) (N-Term) antibodyPEX1 适用: 人, 小鼠 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
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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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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
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别名
- Peroxin 1 / PEX1
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背景
- This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.Synonyms: Peroxin-1, Peroxisome biogenesis disorder protein 1, Peroxisome biogenesis factor 1
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分子量
- 142867 Da
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基因ID
- 5189
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NCBI登录号
- NP_000457
抗原
-
