Recombinant Full Length Listeria Innocua Serovar 6A Atp Synthase Subunit A(Atpb) Protein, His-Tagged

• Cat.No.: RFL581LF
• Product Overview: Recombinant Full Length Listeria innocua serovar 6a ATP synthase subunit a(atpB) Protein (Q927V8) (1-238aa), fused to N-terminal His tag, was expressed in E. coli.

Specification

• Source: E.coli expression system
• Species: Listeria innocua serovar 6a (strain ATCC BAA-680 / CLIP 11262)
• Tag: His
• Form: Lyophilized powder
• Protein Length: Full Length (1-238)
• AA Sequence: MEEEFPTISLLGIDFNLSNILMITV TCVIVLLIAIICTRNLQRRPTGKQN FIEWVMDFVR GIINSNMDWKTGGRFHVLGITLLMF IFVANMLGLPFQIAINDEVWWRSPT ADPIVTLTLA IMVLGLTHYYGIKMRGFKHYFVGTY FSPMKFLFPLKLVEEFANTLTLGLR LYGNIFAGEV LLTIIATQLAHMNIFVGVLAIIPAL LWQGFSIFIGAIQAYIFTMLTMVYM SHKVSDEH
• Purity: Greater than 90% as determined by SDS-PAGE.
• Notes: Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
• Storage: Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
• Storage Buffer: Tris/PBS-based buffer, 6% Trehalose, pH 8.0
• Reconstitution: We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
• Gene Name: atpB
• Synonyms: atpB; lin2679; ATP synthase subunit a; ATP synthase F0 sector subunit a; F-ATPase subunit 6
• UniProt ID: Q927V8

Gene Information

• Gene Name: atpB
• Synonyms: atpB; lin2679; ATP synthase subunit a; ATP synthase F0 sector subunit a; F-ATPase subunit 6
• UniProt ID: Q927V8

Reviews

12/12/2022

Its consistent repeatability makes ATPB a reliable choice for long-term use in various experimental setups.

01/09/2022

The superior activity of ATPB makes it a reliable choice for long-term use in a variety of experimental setup.

12/30/2020

The reliable performance of protein purity makes it the preferred choice for long-term use in a variety of experimental setup.

Q&As

Do ATPB mutations cause intellectual disability?

Some 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.

How do ATPB mutations affect mitochondrial 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.

What is the frequency of ATPB mutations?

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.

What is the relationship between ATPB gene mutations and skeletal myopathy?

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.

Do ATPB mutations affect other organs and systems?

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.

Do ATPB mutations cause developmental abnormalities?

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.