PEX19 抗体 (N-Term)
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Quick Overview for PEX19 抗体 (N-Term) (ABIN5537304)
抗原
See all PEX19 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 33-61, N-Term
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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 PEX19 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 33-61 amino acids from the N-terminal region of human PEX19.
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亚型
- Ig Fraction
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anti-Peroxisomal Biogenesis Factor 19 (PEX19) antibody
PEX19 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2E4 unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) antibodyPEX19 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) antibodyPEX19 适用: 人, 大鼠, 小鼠 IF 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (C-Term) antibodyPEX19 适用: 人, 大鼠, 小鼠, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- For WB starting dilution is: 1:1000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.45 mg/mL
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缓冲液
- 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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储存方法
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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- PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))
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别名
- PEX19
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背景
- This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). 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. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some 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 of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants.
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分子量
- 33 kDa
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基因ID
- 5824
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UniProt
- P40855
抗原
-
