PHYH 抗体
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- 抗原 See all PHYH 抗体
- PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
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适用
- 人, 小鼠
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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 PHYH antibody is un-conjugated
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应用范围
- Immunofluorescence (IF)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human PHYH (NP_006205.1).
- 亚型
- IgG
- Top Product
- Discover our top product PHYH Primary Antibody
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- 应用备注
- IF 1:10-1:100
- 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
- PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
- 别名
- PHYH (PHYH 产品)
- 别名
- zgc:110203 antibody, LN1 antibody, LNAP1 antibody, PAHX antibody, PHYH1 antibody, RD antibody, AI256161 antibody, AI265699 antibody, Lnap1 antibody, phytanoyl-CoA 2-hydroxylase antibody, phytanoyl-CoA hydroxylase-like antibody, phytanoyl-CoA hydroxylase antibody, PHYH antibody, LOC478001 antibody, phyh antibody, Phyh antibody
- 背景
- 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.
- 分子量
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Observed_MW: 40kDa
Calculated_MW: 27kDa/38kDa
- 基因ID
- 5264
- UniProt
- O14832
- 途径
- Monocarboxylic Acid Catabolic Process
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