Peroxisomal Biogenesis Factor 12 (PEX12) (Middle Region) Peptide
PEX12
适用: 人
宿主: 合成
WB
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- 抗原 See all PEX12 products
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
- 蛋白结构域
- Middle Region
- 宿主
- 人
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资源
- 合成
- 应用范围
- Western Blotting (WB)
- 序列
- SIMFLVLLPY LKVKLEKLVS SLREEDEYSI HPPSSRWKRF YRAFLAAYPF
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- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
- 别名
- zgc:56182 Peptide, pex12 Peptide, MGC81372 Peptide, PEX12 Peptide, DDBDRAFT_0186545 Peptide, DDBDRAFT_0238076 Peptide, DDB_0186545 Peptide, DDB_0238076 Peptide, LOC100226224 Peptide, PAF-3 Peptide, PBD3A Peptide, Peroxin-12 Peptide, AI451906 Peptide, peroxisomal biogenesis factor 12 Peptide, peroxisomal biogenesis factor 12 L homeolog Peptide, RING zinc finger-containing protein Peptide, pex12 Peptide, PEX12 Peptide, pex12.L Peptide, Pex12 Peptide
- 背景
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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).
Alias Symbols: PAF-3, PBD3A
Protein Size: 167 - 基因ID
- 5193
- NCBI登录号
- NM_000286, NP_000277
- UniProt
- O00623
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