
Thermo Fisher Scientific Arginase 1 (ARG1) Monoclonal Antibody (OTI2E7)
ARG1 단백질을 인식하는 마우스 단클론 항체로, Western blot과 IHC(P)에서 검증됨. 인간, 마우스, 랫트 반응성. 동결건조 형태로 제공되며 PBS + 8% 트레할로오스 완충액에 보관. 연구용으로 세포 내 Arginase-1 발현 분석에 적합.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:8,000 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI2E7 |
| Immunogen | Full length human recombinant protein of human ARG1 (NP_000036) produced in HEK293T cell |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS with 8% trehalose |
| Contains | No preservative |
| Storage Conditions | -20°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
For reconstitution, add 100 µL of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step using Zeba Spin Desalting Columns (7K MWCO, 0.5 mL, Product #89882).
Target Information
Arginase-1 (Arg1) is a 35 kDa enzyme that catalyzes the conversion of L-arginine to urea and L-ornithine, the final step in the urea cycle. The resulting polyamines are essential for cell proliferation and detoxification of protein degradation byproducts.
By degrading arginine, Arginase 1 limits nitric oxide synthesis by depriving NO synthase of its substrate, thereby down-regulating NO production.
In both humans and mice, Arginase 1 is expressed in the liver, neutrophils, myeloid-derived suppressor cells (MDSCs), and neural stem cells.
In humans, it is expressed in blood neutrophils but not in CCR3+ granulocytes. In mice, Arginase 1 expression is a hallmark of alternatively activated macrophages (M2a).
It may also be expressed in tumor-infiltrating myeloid cells and is commonly detected in hepatocellular carcinoma.
Defects in the ARG1 gene cause argininemia, an autosomal recessive disorder characterized by hyperammonemia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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