PEX26 抗体
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- 抗原 See all PEX26 抗体
- PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This PEX26 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (IF)
- 交叉反应
- 人
- 产品特性
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Rabbit Polyclonal antibody to PEX26 (peroxisomal biogenesis factor 26)
PEX26 antibody - 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Full length human PEX26 Recombinant protein.
- 亚型
- IgG
- Top Product
- Discover our top product PEX26 Primary Antibody
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- 应用备注
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
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Positive Control: A431
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
- 别名
- peroxisomal biogenesis factor 26 (PEX26 产品)
- 别名
- fk41g06 antibody, zgc:64014 antibody, wu:fk41g06 antibody, PBD7A antibody, PBD7B antibody, PEX26M1T antibody, Pex26pM1T antibody, 4632428M11Rik antibody, AI853212 antibody, peroxisomal biogenesis factor 26 antibody, peroxisomal biogenesis factor 26 L homeolog antibody, pex26 antibody, PEX26 antibody, pex26.L antibody, Pex26 antibody
- 背景
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This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Two transcript variants encoding the same protein have been identified for this gene.
Cellular Localization: Peroxisome membrane, Single-pass type II membrane protein - 分子量
- 34 kDa
- 基因ID
- 55670
- UniProt
- Q7Z412
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