PEX13 抗体 (AA 342-403)
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- 抗原 See all PEX13 抗体
- PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))
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抗原表位
- AA 342-403
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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 PEX13 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Synthetic peptide contain a sequence corresponding to a region within amino acids 342 and 403 of Human PEX13
- Top Product
- Discover our top product PEX13 Primary Antibody
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anti-Peroxisomal Biogenesis Factor 13 (PEX13) (AA 1-130) antibody
PEX13 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 13 (PEX13) (C-Term) antibodyPEX13 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 13 (PEX13) (C-Term) antibodyVerified PEX13 适用: 人 ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
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- 应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000 - 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
- 储存条件
- 4 °C/-20 °C
- 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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- 抗原
- PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))
- 别名
- Peroxin 13 (PEX13 产品)
- 别名
- CG4663 antibody, DmelPex13 antibody, Dmel\\CG4663 antibody, pex13 antibody, zgc:66124 antibody, PAS20 antibody, DDBDRAFT_0191662 antibody, DDBDRAFT_0238077 antibody, DDB_0191662 antibody, DDB_0238077 antibody, NALD antibody, PBD11A antibody, PBD11B antibody, ZWS antibody, 2610008O20Rik antibody, Peroxin 13 antibody, peroxisomal biogenesis factor 13 antibody, peroxin PEX13 antibody, peroxin 13 (predicted) antibody, peroxin antibody, SH3 domain-containing protein antibody, putative peroxin 13 antibody, peroxisome biogenesis factor 13 antibody, Pex13 antibody, pex13 antibody, PEX13 antibody
- 背景
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This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm.Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome.[provided by RefSeq]
- 分子量
- 44 kDa
- 基因ID
- 5194
- NCBI登录号
- NM_002618, NP_002609
- 途径
- Feeding Behaviour, Monocarboxylic Acid Catabolic Process
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