anti-Arginase 1 antibody
Key features and details
- 产品描述:
- 反应物种:
- 预测物种:
- 应用:
- 宿主:
- 克隆:
- 同位型:
- 靶点名称:
- 抗原物种:
-
Brand:
CAT.NO. : ARG64816
US＄ Please choose
US＄ Please choose
Size:
Trail, Bulk size or Custom requests Please contact us
Product Details
概述
| 产品描述 | Goat Polyclonal antibody recognizes Arginase 1 |
|---|---|
| 反应物种 | Hu, Ms, Rat, Pig |
| 预测物种 | Cow, Dog |
| 应用 | IHC-P, WB |
| 宿主 | Goat |
| 克隆 | Polyclonal |
| 同位型 | IgG |
| 靶点名称 | Arginase 1 |
| 抗原物种 | Human |
| 抗原 | CFGLAREGNHKPID |
| 偶联标记 | Un-conjugated |
| 別名 | EC 3.5.3.1; Type I arginase; Arginase-1; Liver-type arginase |
应用说明
| 应用建议 |
| ||||||
|---|---|---|---|---|---|---|---|
| 应用说明 | IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0). WB: Recommend incubate at RT for 1h. * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. | ||||||
| 实际分子量 | 37 kDa |
属性
| 形式 | Liquid |
|---|---|
| 纯化 | Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide. |
| 缓冲液 | Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA |
| 抗菌剂 | 0.02% Sodium azide |
| 稳定剂 | 0.5% BSA |
| 浓度 | 0.5 mg/ml |
| 存放说明 | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
| 注意事项 | For laboratory research only, not for drug, diagnostic or other use. |
生物信息
| 数据库连接 | |
|---|---|
| 背景介绍 | Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
| 研究领域 | Metabolism antibody; Signaling Transduction antibody |
| 预测分子量 | 35 kDa |
检测图片 (3)
ARG64816 anti-Arginase 1 antibody IHC-P image
Immunohistochemistry: Paraffin-embedded Human liver stained with ARG64816 anti-Arginase 1 antibody at 3.75 µg/ml dilution. Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
ARG64816 anti-Arginase 1 antibody WB image
Western blot: 35 µg of Human liver lysate (in RIPA buffer) stained with ARG64816 anti-Arginase 1 antibody at 0.01 µg/ml dilution and incubated at RT for 1 hour.
ARG64816 anti-Arginase 1 antibody WB image
Western blot: 35 µg of Pig liver, Mouse liver and Rat liver lysates (in RIPA buffer) stained with ARG64816 anti-Arginase 1 antibody at 0.03 µg/ml dilution and incubated at RT for 1 hour.
New Products
