IMPAD1 抗体 (AA 81-180)
-
- 抗原 See all IMPAD1 抗体
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
-
抗原表位
- AA 81-180
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This IMPAD1 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human IMPAD1
- 亚型
- IgG
- Top Product
- Discover our top product IMPAD1 Primary Antibody
-
anti-Inositol Monophosphatase Domain Containing 1 (IMPAD1) (AA 1-359) antibody
IMPAD1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Inositol Monophosphatase Domain Containing 1 (IMPAD1) (AA 71-120) antibodyIMPAD1 适用: 人, 大鼠, 兔, 犬, 斑马鱼, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-Inositol Monophosphatase Domain Containing 1 (IMPAD1) (AA 215-264) antibodyIMPAD1 适用: 人, 大鼠, 小鼠, 兔, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Inositol Monophosphatase Domain Containing 1 (IMPAD1) (N-Term) antibodyIMPAD1 适用: 人, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
-
- 抗原
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
- 别名
- Impad1 (IMPAD1 产品)
- 背景
-
Synonyms: IMP 3, IMPA3, IMPase 3, Inositol monophosphatase domain containing protein 1, Myo inositol monophosphatase A3.
Background: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
- 基因ID
- 54928
- 途径
- Glycosaminoglycan Metabolic Process
-
