ASS1 (196-212) Goat Polyclonal Antibody
Other products for "ASS1"
Specifications
| Product Data | |
| Applications | ELISA, IHC, IP, WB |
| Recommended Dilution | ELISA: 1/64000. Immunohistochemistry on Paraffin Sections: 2.5 µg/ml. Immunoprecipitation. Western Blot: 0.01 - 0.03 µg/ml. |
| Reactivities | Bat, Bovine, Canine, Equine, Human, Monkey, Mouse, Porcine, Rat |
| Host | Goat |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide from an internal region of human ASS1 |
| Specificity | This antibody detects ASS1 (Internal). |
| Formulation | Tris saline buffer, pH 7.3, 0.5% BSA, 0.02% sodium azide State: Aff - Purified State: Liquid Ig fraction |
| Concentration | lot specific |
| Purification | Immunoaffinity chromatography |
| Storage | Store at 2 - 8 °C for up to one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing. |
| Stability | Shelf life: one year from despatch. |
| Gene Name | Homo sapiens argininosuccinate synthase 1 (ASS1), transcript variant 1 |
| Database Link | |
| Background | Arginosuccinate synthetase catalyzes the penultimate step of the arginine biosynthetic pathway. There are approximately 10 to 14 ASS pseudogenes scattered across the human genome; the ASS gene located on chromosome 9 appears to be the only functional gene for argininosuccinate synthetase. The ASS primary transcript is subject to alternative splicing in the 5' non-coding region; a splice variant lacking exon 2 occurs in liver and fibroblast cells. Mutations in the chromosome 9 copy of ASS cause citrullinemia. |
| Synonyms | Argininosuccinate synthase |
| Reference Data | |
| Protein Families | Druggable Genome |
| Protein Pathways | Alanine, aspartate and glutamate metabolism, Arginine and proline metabolism, Metabolic pathways |
Documents
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