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- 抗原 See all PEX12 抗体
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
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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 PEX12 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human PEX12 (NP_000277.1).
- 亚型
- IgG
- Top Product
- Discover our top product PEX12 Primary Antibody
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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 1-359) antibodyPEX12 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 12 (PEX12) (AA 290-359) antibodyPEX12 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
- 别名
- PEX12 (PEX12 产品)
- 别名
- zgc:56182 antibody, pex12 antibody, MGC81372 antibody, PEX12 antibody, DDBDRAFT_0186545 antibody, DDBDRAFT_0238076 antibody, DDB_0186545 antibody, DDB_0238076 antibody, LOC100226224 antibody, PAF-3 antibody, PBD3A antibody, Peroxin-12 antibody, AI451906 antibody, peroxisomal biogenesis factor 12 antibody, peroxisomal biogenesis factor 12 L homeolog antibody, RING zinc finger-containing protein antibody, pex12 antibody, PEX12 antibody, pex12.L antibody, Pex12 antibody
- 背景
- This gene 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).
- 分子量
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Observed_MW: 41 kDa
Calculated_MW: 40 kDa
- 基因ID
- 5193
- UniProt
- O00623
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