Recombinant Mouse ACO2 Protein, GST & His-tagged
Cat.No. : | ACO2-950M |
Product Overview : | Recombinant mouse ACO2 (Q99KI0) (Gln 28-Gln 780) was fused with the N-terminal polyhistidine-tagged GST tag at the N-terminus. |
- Specification
- Gene Information
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Source : | Baculovirus-Insect Cells |
Species : | Mouse |
Tag : | GST & His |
Predicted N Terminal : | Met |
Form : | Lyophilized from sterile 50mM Tris, 100mM NaCl, 10% gly, 0.5mM GSH, pH 8.01, 5%~8% trehalose and mannitol. |
Molecular Mass : | The secreted recombinant mouse ACO2/GST chimera consists of 990 amino acids and has a calculated molecular mass of 110 kDa. The recombinant protein migrates as an approximately 100 kDa band in SDS-PAGE under reducing conditions. |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method. |
Purity : | >90 % as determined by SDS-PAGE. |
Stability : | Samples are stable for up to twelve months from date of receipt at -70ºC. |
Storage : | Store it under sterile conditions at -20ºC~-70ºC. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
Reconstitution : | It is recommended that sterile water be added to the vial to prepare a stock solution of 0.25 ug/ul. Centrifuge the vial at 4℃ before opening to recover the entire contents. |
Gene Name : | Aco2 aconitase 2, mitochondrial [ Mus musculus ] |
Official Symbol : | ACO2 |
Synonyms : | ACO2; aconitase 2, mitochondrial; aconitate hydratase, mitochondrial; citrate hydro-lyase; Aco3; Aco-2; D10Wsu183e; |
Gene ID : | 11429 |
mRNA Refseq : | NM_080633 |
Protein Refseq : | NP_542364 |
MIM : | |
UniProt ID : | |
Pathway : | Citrate cycle (TCA cycle), organism-specific biosystem; Citrate cycle (TCA cycle), conserved biosystem; Citrate cycle, first carbon oxidation, oxaloacetate =>2-oxoglutarate, organism-specific biosystem; Citrate cycle, first carbon oxidation, oxaloacetate |
Function : | 3 iron, 4 sulfur cluster binding; 4 iron, 4 sulfur cluster binding; aconitate hydratase activity; aconitate hydratase activity; citrate hydro-lyase (cis-aconitate-forming) activity; iron ion binding; iron-sulfur cluster binding; isocitrate hydro-lyase (ci |
Products Types
◆ Recombinant Protein | ||
ACO2-38R | Recombinant Rhesus Macaque ACO2 Protein, His (Fc)-Avi-tagged | +Inquiry |
ACO2-914H | Recombinant Human ACO2 Protein, MYC/DDK-tagged | +Inquiry |
ACO2-111R | Recombinant Rat ACO2 Protein, His (Fc)-Avi-tagged | +Inquiry |
Aco2-513M | Recombinant Mouse Aco2 Protein, MYC/DDK-tagged | +Inquiry |
ACO2-258H | Recombinant Human ACO2 Protein, His (Fc)-Avi-tagged | +Inquiry |
◆ Lysates | ||
ACO2-440MCL | Recombinant Mouse ACO2 cell lysate | +Inquiry |
ACO2-498HCL | Recombinant Human ACO2 cell lysate | +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 (10)
Ask a questionACO2 is involved in the TCA cycle, which is a critical process for energy production in cells. Specifically, it catalyzes the conversion of citrate to isocitrate, which is a crucial step in the cycle.
Yes, mutations in the ACO2 gene have been associated with several disorders, including infantile cerebellar-retinal degeneration and mitochondrial encephalopathy. These conditions are characterized by a range of symptoms, including neurological and developmental abnormalities.
ACO2 is a potential target for cancer treatment, as it is overexpressed in several types of cancer cells. However, the development of drugs that target ACO2 is still in the early stages of research.
ACO1 and ACO2 are two isoforms of aconitate hydratase, which catalyze the same reaction in the TCA cycle. However, ACO2 is primarily located in the mitochondria of cells, while ACO1 is located in the cytoplasm.
Unlike ACO1, ACO2 is not involved in iron metabolism. Its role is primarily in energy production through the TCA cycle.
ACO2 deficiency has been associated with several disorders, including infantile cerebellar-retinal degeneration and mitochondrial encephalopathy. These conditions are characterized by various neurological and developmental abnormalities.
ACO2 is a homodimeric enzyme composed of two identical subunits. Each subunit contains a catalytic domain and a regulatory domain, which work together to catalyze the isomerization of citrate to isocitrate.
ACO2 activity can be measured in the laboratory using a variety of techniques, including spectrophotometric assays and enzymatic activity assays. These assays typically involve measuring the rate of citrate isomerization to isocitrate in the presence of ACO2 and other necessary cofactors.
ACO2 activity is regulated by a variety of factors, including substrate availability, pH, and post-translational modifications such as phosphorylation. Additionally, ACO2 activity can be modulated by other enzymes and metabolic pathways in the cell.
While ACO2 is primarily known for its role in energy production, recent research suggests that it may also play a role in other cellular processes. For example, studies have shown that ACO2 may be involved in regulating the immune response and cellular metabolism.
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