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Recombinant Full Length Human ACO2 Protein, C-Flag-tagged

Cat.No. : ACO2-1215HFL
Product Overview : Recombinant Full Length Human ACO2 Protein, fused to Flag-tag at C-terminus, was expressed in Mammalian cells.
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Description : The protein encoded by this gene belongs to the aconitase/IPM isomerase family. It is an enzyme that catalyzes the interconversion of citrate to isocitrate via cis-aconitate in the second step of the TCA cycle. This protein is encoded in the nucleus and functions in the mitochondrion. It was found to be one of the mitochondrial matrix proteins that are preferentially degraded by the serine protease 15(PRSS15), also known as Lon protease, after oxidative modification.
Source : Mammalian cells
Species : Human
Tag : Flag
Form : 25 mM Tris HCl, pH 7.3, 100 mM glycine, 10% glycerol.
Molecular Mass : 82.4 kDa
AA Sequence : MAPYSLLVTRLQKALGVRQYHVASV LCQRAKVAMSHFEPNEYIHYDLLEK NINIVRKRLNRPLTLSEKIV YGHLDDPASQEIERGKSYLRLRPDR VAMQDATAQMAMLQFISSGLSKVAV PSTIHCDHLIEAQVGGEKDL RRAKDINQEVYNFLATAGAKYGVGF WKPGSGIIHQIILENYAYPGVLLIG TDSHTPNGGGLGGICIGVGG ADAVDVMAGIPWELKCPKVIGVKLT GSLSGWSSPKDVILKVAGILTVKGG TGAIVEYHGPGVDSISCTGM ATICNMGAEIGATTSVFPYNHRMKK YLSKTGREDIANLADEFKDHLVPDP GCHYDQLIEINLSELKPHIN GPFTPDLAHPVAEVGKVAEKEGWPL DIRVGLIGSCTNSSYEDMGRSAAVA KQALAHGLKCKSQFTITPGS EQIRATIERDGYAQILRDLGGIVLA NACGPCIGQWDRKDIKKGEKNTIVT SYNRNFTGRNDANPETHAFV TSPEIVTALAIAGTLKFNPETDYLT GTDGKKFRLEAPDADELPKGEFDPG QDTYQHPPKDSSGQHVDVSP TSQRLQLLEPFDKWDGKDLEDLQIL IKVKGKCTTDHISAAGPWLKFRGHL DNISNNLLIGAINIENGKAN SVRNAVTQEFGPVPDTARYYKKHGI RWVVIGDENYGEGSSREHAALEPRH LGGRAIITKSFARIHETNLK KQGLLPLTFADPADYNKIHPVDKLT IQGLKDFTPGKPLKCIIKHPNGTQE TILLNHTFNETQIEWFRAGS
ALNRMKELQQTRTRPLEQKLISEED LAANDILDYKDDDDKV
Purity : > 80% as determined by SDS-PAGE and Coomassie blue staining.
Stability : Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
Storage : Store at -80 centigrade.
Concentration : >50 ug/mL as determined by microplate BCA method.
Preparation : Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps.
Protein Pathways : Citrate cycle (TCA cycle), Glyoxylate and dicarboxylate metabolism, Metabolic pathways
Gene Name : ACO2 aconitase 2 [ Homo sapiens (human) ]
Official Symbol : ACO2
Synonyms : ICRD; OCA8; OPA9; ACONM; HEL-S-284
Gene ID : 50
mRNA Refseq : NM_001098.3
Protein Refseq : NP_001089.1
MIM : 100850
UniProt ID : Q99798

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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What is the function of ACO2? 12/29/2022

ACO2 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.

Can ACO2 mutations cause disease? 12/11/2022

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.

Can ACO2 be targeted for medical treatment?  10/05/2021

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.

How does ACO2 differ from ACO1? 04/28/2021

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.

Is ACO2 involved in iron metabolism? 10/30/2018

Unlike ACO1, ACO2 is not involved in iron metabolism. Its role is primarily in energy production through the TCA cycle.

What happens if ACO2 is deficient? 09/26/2018

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.

What is the structure of ACO2? 06/23/2018

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.

How is ACO2 measured in the laboratory?  10/02/2017

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.

How is the activity of ACO2 regulated? 09/29/2017

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.

Does ACO2 have any other functions in addition to energy production? 06/30/2015

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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