Recombinant Bacillus subtilis ATPB protein, His-tagged
Cat.No. : | ATPB-1743B |
Product Overview : | Recombinant Bacillus subtilis ATPB full length or partial length protein was expressed. |
- Specification
- Gene Information
- Related Products
Source : | E. coli or Yeast |
Species : | Bacillus subtilis |
Tag : | His |
Form : | Liquid or lyophilized powder |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method. |
Purity : | > 80% by SDS-PAGE |
Notes : | This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications. |
Storage : | Store it at +4 ºC for short term. For long term storage, store it at -20 ºC~-80 ºC. |
Storage buffer : | PBS buffer |
Gene Name : | atpB ATP synthase subunit a [ Bacillus subtilis subsp. subtilis str. 168 ] |
Official Symbol : | ATPB |
Synonyms : | ATPB; ATP synthase subunit a |
Gene ID : | 937004 |
UniProt ID : | P37813 |
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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 questionSome ATPB gene mutations may be associated with intellectual disability. Since the F1 subunit of ATP synthase is involved in the process of cellular energy synthesis, mutations in the ATPB gene may result in insufficient cellular energy supply and thus affect brain function.
ATPB gene mutations may lead to impaired mitochondrial function and affect intracellular energy metabolism. Mitochondria are the energy production centers in cells, and impaired mitochondrial function may lead to insufficient cellular energy supply and affect the normal function of multiple tissues and organs.
The frequency of ATPB gene mutations varies among different populations and regions. Because ATPB gene mutations are often associated with rare genetic disorders, their frequency in the overall population is relatively low.
Some ATPB gene mutations may lead to skeletal myopathy. This is due to the high dependence of skeletal muscle on energy supply, and the abnormal cellular energy metabolism caused by ATPB gene mutations may further affect the function and health of skeletal muscle.
ATPB mutations may affect the function of multiple organs and systems. In addition to mitochondria and skeletal muscle, other tissues that depend on ATP supply, such as the nervous system, heart, and liver, among others, may also be affected.
Certain ATPB gene mutations may lead to developmental abnormalities, especially during embryonic development. This can involve multiple organs and systems, leading to problems such as birth defects and developmental delays.
Customer Reviews (3)
Write a reviewIts consistent repeatability makes ATPB a reliable choice for long-term use in various experimental setups.
The superior activity of ATPB makes it a reliable choice for long-term use in a variety of experimental setup.
The reliable performance of protein purity makes it the preferred choice for long-term use in a variety of experimental setup.
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