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Produkt-Information von ARG1 / Arginase 1 Antikörper
| Immunogen | Recombinant Human ARG1 / Arginase 1 protein (Catalog#11558-H08H) |
| Antibody Type | Rabbit Polyclonal Antibody ( Antibody Purification Platform ) |
| Ig Type | Rabbit IgG |
| Formulation | 0.2 μm filtered solution in PBS with 5% trehalose |
| Preparation | Produced in rabbits immunized with purified, recombinant Human ARG1 / Arginase 1 (rh ARG1 / Arginase 1; Catalog#11558-H08H; P05089-1; Met 1-Lys 322). Total IgG was purified by Protein A affinity chromatography. |
ARG1 / Arginase 1 Antikörper Usage Guide
| Specificity | Human ARG1 / Arginase 1 |
| Western blot | This antibody can be used at 1-2 μg/mL with the appropriate secondary reagents to detect Human ARG1 in WB. |
| Direct ELISA | This antibody can be used at 0.5-1 μg/mL with the appropriate secondary reagents to detect Human ARG1. The detection limit for Human ARG1 is approximately 0.0049 ng/well. |
| Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -70℃. Preservative-Free. Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles. |
Verwandte Produkte & Themen von ARG1 / Arginase 1 Antikörper
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Hintergrund von ARG1 / Arginase 1 Antikörper
Arginase-1, also known as Liver-type arginase, Type I arginase and ARG1 is a cytoplasm protein which belongs to thearginase family. Arginase-1 / ARG1 is a manganese-containing enzyme. The reaction catalyzed by this enzyme is: arginine + H2O → ornithine + urea. It is the final enzyme of the urea cycle. Arginase-1 / ARG1 is the fifth and final step in the urea cycle, a series of biophysical reactions in mammals during which the body disposes of harmful ammonia. Specifically, Arginase-1 / ARG1 converts L-arginine into L-ornithine and urea. In most mammals, two isozymes of this enzyme exist; the first, Arginase-1 / ARG1, functions in the urea cycle, and is located primarily in the cytoplasm of the liver. The second isozyme, Arginase-2 / ARG2, has been implicated in the regulation of the arginine/ornithine concentrations in the cell. It is located in mitochondria of several tissues in the body, with most abundance in the kidney and prostate. Defects in Arginase-1 / ARG1 are the cause of argininemia (ARGIN), also known as hyperargininemia. Argininemia is a rare autosomal recessive disorder of the urea cycle. Arginine is elevated in the blood and cerebrospinal fluid, and periodic hyperammonemia occurs.
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