Recombinant Mouse ATP9A Protein Pre-coupled Magnetic Beads
Cat.No. : | ATP9A-890M-B |
Product Overview : | The Recombnant protein was conjugated to magnetic beads. This ready-to-use, pre-coupled magnetic beads are in uniform particle size and narrow size distribution with large surface area, which is conducive to convenient and fast capture target molecules with high specificity and achieve magnetic separation. This product can be equipped with automation equipment for high-throughput operations. |
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Source : | HEK293 |
Species : | Mouse |
Form : | Solution |
Particle size : | ~2 μm |
Beads Surface : | Hydrophilic |
Capacity : | > 200 pmol rabbit IgG/ mg beads |
Applications : | Immunoassay, In vitro diagnostics, cell sorting, Immunoprecipitation/Co-precipitation, Protein/antibody separation and purification. |
Stability : | Stable for at least 6 months from the date of receipt of the product under proper storage and handling conditions. |
Storage : | 2-8℃. Do not to freeze thaw the Beads |
Concentration : | 10mg beads/mL |
Storage Buffer : | PBS buffer |
Gene Name : | Atp9a ATPase, class II, type 9A [ Mus musculus ] |
Official Symbol : | ATP9A |
Gene ID : | 11981 |
mRNA Refseq : | NM_015731.3 |
Protein Refseq : | NP_056546.2 |
UniProt ID : | O70228 |
Products Types
◆ Recombinant Protein | ||
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ATP9A-1018H | Recombinant Human ATP9A protein, GST-tagged | +Inquiry |
ATP9A-2180M | Recombinant Mouse ATP9A Protein | +Inquiry |
Related Gene
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (6)
Ask a questionATP9A gene is widely expressed in various human tissues. However, its expression levels may vary in different tissues and cell types.
Detection of ATP9A gene mutations is usually performed by gene sequencing technology. Common methods include Sanger sequencing, next generation sequencing (NGS), etc. These methods can detect point mutations, insertion/deletion mutations and so on on ATP9A gene.
The protein is involved in the phospholipid turnover process of cell membrane and maintains the stability of cell membrane. ATP9A gene mutation may lead to abnormal protein function, and then affect the stability of cell membrane.
Currently, there is no specific therapy targeting ATP9A gene mutations. However, understanding the mutation status of ATP9A gene can help doctors better understand the disease risk and prognosis of patients to develop individualized treatment plans.
This gene mutation may lead to the structural and functional abnormalities of ATP9A protein, affecting the phospholipid turnover process of the inner and outer membranes of cells. This may negatively affect the function and stability of the cells.
The effects of specific ATP9A gene mutations on nervous system development are unknown. However, several studies have shown that ATP9A protein plays an important role in nerve cells, and mutations may be associated with intellectual disability and neurodevelopmental abnormalities.
Customer Reviews (3)
Write a reviewThe stability of ATP9A is very stable under a variety of environmental conditions, whether it is low temperature, high temperature, or other extreme environments, and its performance remains consistent.
As the production process of ATP9A adopts the most advanced biotechnology, the production process is more green and sustainable.
Due to the short half-life and high clearance rate of recombinant proteins, their rapid clearance from the body reduces the risk of side effects.
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