DPM1 抗体
Quick Overview for DPM1 抗体 (ABIN7263775)
抗原
See all DPM1 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein of human DPM1 (NP_003850.1).
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亚型
- IgG
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anti-Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1) (AA 2-260) antibody
DPM1 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1) (N-Term) antibodyVerified DPM1 适用: 人 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1) (AA 1-260) antibodyDPM1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1) (N-Term) antibodyVerified DPM1 适用: 大鼠 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1) (Center) antibodyDPM1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1) antibodyDPM1 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- IF 1:50-1:200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- DPM1 (Dolichyl-Phosphate Mannosyltransferase Polypeptide 1, Catalytic Subunit (DPM1))
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别名
- DPM1
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背景
- Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. Human DPM1 lacks a carboxy-terminal transmembrane domain and signal sequence and is regulated by DPM2. Mutations in this gene are associated with congenital disorder of glycosylation type Ie. Alternative splicing results in multiple transcript variants.
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基因ID
- 8813
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UniProt
- O60762
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途径
- Inositol Metabolic Process
抗原
-
