Phytanoyl-CoA 2-Hydroxylase (PHYH) (Middle Region) Peptide
PHYH
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all PHYH products
- PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
- 蛋白结构域
- Middle Region
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 序列
- VVLPGTHKGS LKPHDYPKWE GGVNKMFHGI QDYEENKARV HLVMEKGDTV
- 产品特性
- This is a synthetic peptide designed for use in combination with anti- PHYH Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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- 应用备注
- Optimal working dilution should be determined by the investigator.
- 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
- PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
- 别名
- zgc:110203 Peptide, LN1 Peptide, LNAP1 Peptide, PAHX Peptide, PHYH1 Peptide, RD Peptide, AI256161 Peptide, AI265699 Peptide, Lnap1 Peptide, phytanoyl-CoA 2-hydroxylase Peptide, phytanoyl-CoA hydroxylase-like Peptide, phytanoyl-CoA hydroxylase Peptide, PHYH Peptide, LOC478001 Peptide, phyh Peptide, Phyh Peptide
- 背景
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This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Alias Symbols: RD, LN1, PAHX, LNAP1, PHYH1
Protein Size: 338 - 基因ID
- 5264
- NCBI登录号
- NM_001037537, NP_006205
- UniProt
- O14832
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