ATP7A
Product Sizes
25ul
£177.00
ARP33797-T100-25UL
100 ul
£373.00
ARP33797-T100-100UL
About this Product
- SKU:
- ARP33797-T100
- Additional Names:
- MK; MNK; DSMAX; SMAX3
- Clonality:
- Polyclonal
- Concentration:
- 1.0 mg/ml
- Extra Details:
- The ATP7A gene encodes the Menkes copper-translocating P-type ATPase; a ubiquitous protein that regulates the absorption of copper in the gastrointestinal tract. Inside cells; this protein has a dual function: it delivers copper to cuproenzymes in the Golgi compartment and effluxes excess copper. The trafficking mechanism and catalytic activity combine to facilitate absorption and intercellular transport of copper. Menkes disease; a systemic copper deficiency disorder; is caused by mutations in the ATP7A gene.
- Gene Details:
- ATPase; Cu++ transporting; alpha polypeptide
- Host:
- Rabbit
- Immunogen:
- The immunogen is a synthetic peptide directed towards the N terminal region of human ATP7A
- Molecular Weight:
- 163kDa
- Protein Details:
- ATP7A protein EMBL BAC82353.1
- Purification:
- Protein A purified
- Shipping Conditions:
- Blue Ice
- Storage Conditions:
- For short term use; store at 2-8C up to 1 week. For long term storage; store at -20C in small aliquots to prevent freeze-thaw cycles.
- Supplier:
- Aviva Systems Biology
- Type:
- Antibodies: Polyclonal Antibody
- Manufacturer's Data Sheet:html_datasheet.php
