PEX12 抗体 (AA 180-260)
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Quick Overview for PEX12 抗体 (AA 180-260) (ABIN7230590)
抗原
See all PEX12 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 180-260
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原理
- PEX12 Polyclonal Antibody
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特异性
- The antibody detects endogenous levels of PEX12 protein
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纯化方法
- The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen
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免疫原
- Synthesized peptide derived from part region of human PEX12 protein at AA range: 180-260
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亚型
- IgG
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anti-Peroxisomal Biogenesis Factor 12 (PEX12) (Internal Region) antibody
PEX12 适用: 人, 小鼠, 大鼠 WB, ELISA, ICC, IF, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 290-359) antibodyPEX12 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 1-359) antibodyPEX12 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).
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说明
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Primary Antibody
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.
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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
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
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别名
- PEX12
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背景
- Rabbit Anti-PEX12 Polyclonal Antibody,Peroxisome assembly protein 12, Peroxin-12, Peroxisome assembly factor 3, PAF-3,PEX12 (Peroxisomal Biogenesis Factor 12) is a Protein Coding gene. Diseases associated with PEX12 include Peroxisome Biogenesis Disorder 3B and Peroxisome Biogenesis Disorder 3A. Among its related pathways are Peroxisome. PEX12 belongs to the peroxin-12 family. 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 of Zellweger syndrome (ZWS).,PEX12
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分子量
- observerd band 39kDa
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基因ID
- 5193
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UniProt
- O00623
抗原
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