PEX3 抗体
Quick Overview for PEX3 抗体 (ABIN7117349)
抗原
See all PEX3 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Immunogen affinity purified
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纯度
- ≥95 % as determined by SDS-PAGE
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免疫原
- peroxisomal biogenesis factor 3
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亚型
- IgG
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anti-Peroxisomal Biogenesis Factor 3 (PEX3) (N-Term) antibody
PEX3 适用: 人, 小鼠, 大鼠, 犬 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (N-Term) antibodyPEX3 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (AA 144-373) antibodyPEX3 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (AA 31-80) antibodyPEX3 适用: 人, 小鼠, 大鼠, Cow, 犬, 猴, 豚鼠, 马, 兔, Bat, 小鸡, Hamster, Pig, 非洲爪蟾 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (N-Term) antibodyPEX3 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (N-Term) antibodyPEX3 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (N-Term) antibodyPEX3 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (AA 1-373) antibodyPEX3 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 3 (PEX3) (AA 271-373) antibodyPEX3 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 3C2 unconjugated
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应用备注
- WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
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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
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
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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
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
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有效期
- 12 months
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- PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))
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别名
- PEX3
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背景
- Synonyms: Background:The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS).
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分子量
- 37 kDa
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基因ID
- 8504
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UniProt
- P56589
抗原
-
