PEX26 抗体 (AA 1-265)
Quick Overview for PEX26 抗体 (AA 1-265) (ABIN1885866)
抗原
See all PEX26 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 1-265
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 265 of Human PEX26
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anti-Peroxisomal Biogenesis Factor 26 (PEX26) (AA 1-159) antibody
PEX26 适用: 人 WB, ELISA, IHC, IP 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 26 (PEX26) antibodyPEX26 适用: 人 WB, ICC, IHC (p), IF 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 26 (PEX26) (AA 1-305) antibodyPEX26 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 26 (PEX26) (N-Term) antibodyPEX26 适用: 人, Cow, 小鼠, 大鼠, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 26 (PEX26) (AA 179-228) antibodyPEX26 适用: 人, Cow, 马 WB 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 26 (PEX26) (Internal Region) antibodyVerified PEX26 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 26 (PEX26) (N-Term) antibodyPEX26 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 26 (PEX26) (Middle Region) antibodyPEX26 适用: 人, Cow, Pig, 马 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.500
Immunofluorescence: 1.100-1.200 -
限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
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储存液
- Thimerosal (Merthiolate)
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注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
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别名
- Peroxin 26
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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.[provided by RefSeq]
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分子量
- 34 kDa
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基因ID
- 55670
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NCBI登录号
- NP_060399, NM_017929
抗原
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