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Anti-PRTFDC1 Antibody (1M206)
😃Good
Catalog No. TMAY-02683
Alias PRTFDC1, phosphoribosyl transferase domain containing 1, HHGP
Anti-PRTFDC1 Antibody (1M206) is a Rabbit antibody targeting PRTFDC1. Anti-PRTFDC1 Antibody (1M206) can be used in ELISA.
Anti-PRTFDC1 Antibody (1M206)
Anti-PRTFDC1 Antibody (1M206)
😃Good
Catalog No. TMAY-02683Alias PRTFDC1, phosphoribosyl transferase domain containing 1, HHGP
Anti-PRTFDC1 Antibody (1M206) is a Rabbit antibody targeting PRTFDC1. Anti-PRTFDC1 Antibody (1M206) can be used in ELISA.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 100 μL | $268 | 7-10 days | 7-10 days |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Related Conjugates and Formulations
Antigen Details
Chemical Properties
| Description | Anti-PRTFDC1 Antibody (1M206) is a Rabbit antibody targeting PRTFDC1. Anti-PRTFDC1 Antibody (1M206) can be used in ELISA. |
| Synonyms | PRTFDC1, phosphoribosyl transferase domain containing 1, HHGP |
| Ig Type | Rabbit IgG |
| Clone | 1M206 |
| Reactivity | Human |
| Specificity | Human PRTFDC1 |
| Application | |
| Recommended Dose | ELISA: 1:5000-1:10000 |
| Antibody Type | Monoclonal |
| Host Species | Rabbit |
| Construction | This antibody was obtained from a rabbit immunized with purified, recombinant Human PRTFDC1 (rh PRTFDC1; TMPY-03332; Q9NRG1-1; Met1-Val225). |
| Purification | Protein A |
| Appearance | Liquid |
| Formulation | 0.2 μm filtered solution in PBS |
| Research Background | PRTFDC1 is a member of the purine/pyrimidine phosphoribosyltransferase family. It can bind GMP, IMP and alpha-D-5-phosphoribosyl 1-pyrophosphate (PRPP). The epigenetic silencing of PRTFDC1 by hypermethylation of the CpG island leads to a loss of PRTFDC1 function, which might be involved in squamous cell oral carcinogenesis. PRTFDC1 is a genetic modifier of HPRT-deficiency in the mouse and has important implications for unraveling the molecular etiology of lesch-Nyhan disease(LND). LND is a severe X-linked neurological disorder caused by a deficiency of hypoxanthine phosphoribosyltransferase. PRTFDC1 has a low, barely measurable phosphoribosyltransferase activity (in vitro). |
| Conjucates | Unconjugated |
| Immunogen | Recombinant Protein: Human PRTFDC1 Protein (TMPY-03332) |
| Antigen Species | Human |
Stability & Storage
| Stability & Storage | Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. Preservative-Free. |
| Transport | Shipping with blue ice. |
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