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| Item number | Size | Datasheet | Manual | SDS | Delivery time | Quantity | Price |
|---|---|---|---|---|---|---|---|
| NSJ-FY12660 | 100 µg | - | - |
3 - 10 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. ACP2 antibody detects... more
Product information "Anti-ACP2 / Lysosomal acid phosphatase 2"
Adding 0.2 ml of distilled water will yield a concentration of 500 ug/ml. ACP2 antibody detects Lysosomal acid phosphatase 2, an enzyme responsible for the hydrolysis of phosphate esters within the acidic environment of lysosomes. ACP2 plays an essential role in the degradation of macromolecules, phosphate turnover, and lysosomal homeostasis. It functions as part of a larger lysosomal complex that regulates both nutrient recycling and intracellular signaling. The ACP2 antibody is widely used in cell biology, metabolism, and pathology research to study lysosomal function, enzyme regulation, and metabolic disorders.ACP2 is encoded by the ACP2 gene located on human chromosome 11p11.2. The protein is approximately 452 amino acids in length and is synthesized as a precursor that undergoes proteolytic cleavage into two subunits?a 36 kilodalton alpha subunit and a 14 kilodalton beta subunit?that together form the active enzyme. ACP2 localizes predominantly to the lysosomal lumen but can also be detected in late endosomes and phagosomes, reflecting its involvement in diverse degradative pathways.The ACP2 antibody detects the 50 kilodalton precursor and its processed subunits by western blot and shows punctate lysosomal staining by immunofluorescence microscopy. ACP2 participates in the hydrolysis of phosphate-containing substrates derived from nucleotides, phospholipids, and other macromolecules, releasing inorganic phosphate for metabolic reuse. It complements the function of acid phosphatase ACP3, ensuring redundancy in phosphate metabolism and cellular cleanup.Mutations or deficiencies in ACP2 lead to acid phosphatase deficiency, a rare lysosomal storage disorder characterized by abnormal accumulation of phosphomonoesters and progressive neurodegeneration. Reduced ACP2 activity has also been implicated in osteopetrosis-like bone disorders and altered immune responses, as lysosomal enzymes regulate antigen presentation and macrophage function. Conversely, upregulation of ACP2 is observed during macrophage activation and tissue remodeling, highlighting its adaptive role in immune and metabolic balance.As a lysosomal hydrolase linking phosphate metabolism to intracellular clearance, ACP2 is a valuable marker for lysosome integrity and metabolic health. NSJ Bioreagents provides a validated ACP2 antibody optimized for its applications, supporting research into catabolic pathways, phosphate metabolism, and lysosomal storage diseases.
| Keywords: | Anti-ACP2, Anti-Lysosomal acid phosphatase, ACP2 Antibody / Lysosomal acid phosphatase 2 |
| Supplier: | NSJ Bioreagents |
| Supplier-Nr: | FY12660 |
Properties
| Application: | WB, ELISA |
| Antibody Type: | Polyclonal |
| Conjugate: | No |
| Host: | Rabbit |
| Species reactivity: | human, mouse, rat |
| Immunogen: | E.coli-derived human ACP2 recombinant protein (Position: R31-H88) |
| Format: | Purified |
Database Information
| KEGG ID : | K14410 | Matching products |
| UniProt ID : | P11117 | Matching products |
| Gene ID : | GeneID 53 | 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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