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| Item number | Size | Datasheet | Manual | SDS | Delivery time | Quantity | Price |
|---|---|---|---|---|---|---|---|
| NSJ-FY12495 | 100 µg | - | - |
7 - 12 business days* |
790.00€
|
If you have any questions, please use our Contact Form.
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
Adding 0.2 ml of distilled water will yield a concentration of 500 ug/ml. PCYT2 antibody detects... more
Product information "Anti-PCYT2 / Ethanolamine-phosphate cytidylyltransferase"
Adding 0.2 ml of distilled water will yield a concentration of 500 ug/ml. PCYT2 antibody detects Ethanolamine-phosphate cytidylyltransferase, a key enzyme in the CDP-ethanolamine branch of the Kennedy pathway for phosphatidylethanolamine synthesis. PCYT2 catalyzes the formation of CDP-ethanolamine from CTP and phosphoethanolamine, an essential step in the biosynthesis of membrane phospholipids. The PCYT2 antibody is used in lipid metabolism, neurobiology, and mitochondrial research to study phospholipid homeostasis and membrane biogenesis.PCYT2 is encoded by the PCYT2 gene located on human chromosome 17q25.3. The protein is approximately 43 kilodaltons and localized predominantly in the endoplasmic reticulum. It functions as a rate-limiting enzyme that determines phosphatidylethanolamine synthesis levels, thereby influencing membrane fluidity, mitochondrial morphology, and cellular signaling. PCYT2 activity is critical for maintaining the structural integrity of cell membranes and organelles, particularly in the nervous system and muscle tissue.Using the PCYT2 antibody, researchers can identify the 43 kilodalton protein by western blot and immunofluorescence, where it shows perinuclear localization corresponding to the ER network. Genetic and biochemical studies have shown that PCYT2 deficiency results in reduced phosphatidylethanolamine production, leading to mitochondrial dysfunction, abnormal lipid droplet accumulation, and neurodevelopmental impairment. Mutations in PCYT2 cause hereditary spastic paraplegia type 82 and neuromuscular lipid metabolism disorders.PCYT2 expression is regulated by nutritional and hormonal cues, including insulin and fatty acid levels. It interacts with lipid transfer proteins and participates in the coordination between the Kennedy pathway and mitochondrial phospholipid synthesis. NSJ Bioreagents provides a validated PCYT2 antibody supporting research into membrane biosynthesis, lipid metabolism disorders, and mitochondrial integrity.
| Keywords: | Anti-PCYT2, Anti-Phosphorylethanolamine transferase, Anti-Ethanolamine-phosphate cytidylyltransferase, Anti-CTP:phosphoethanolamine cytidylyltransferase, PCYT2 Antibody / Ethanolamine-phosphate cytidylyltransferase |
| Supplier: | NSJ Bioreagents |
| Supplier-Nr: | FY12495 |
Properties
| Application: | WB, ICC/IF, IP, FC, ELISA |
| Antibody Type: | Polyclonal |
| Conjugate: | No |
| Host: | Rabbit |
| Species reactivity: | human, mouse, rat |
| Immunogen: | E.coli-derived human PCYT2 recombinant protein (Position: D32-F389) |
| Format: | Purified |
Database Information
| KEGG ID : | K00967 | Matching products |
| UniProt ID : | Q99447 | Matching products |
| Gene ID : | GeneID 5833 | Matching products |
Handling & Safety
| Storage: | +4°C |
| Shipping: | +4°C (International: +4°C) |
Caution
Our products are for laboratory research use only: Not for administration to humans!
Our products are for laboratory research use only: Not for administration to humans!
Information about the product reference will follow.
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