Recombinant Mouse Aldoc, His-tagged
Cat.No. : | Aldoc-55M |
Product Overview : | Recombinant mouse Aldoc, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques. |
- Specification
- Gene Information
- Related Products
- Download
Description : | Aldoc also known as fructose-bisphosphate aldolase C, is a member of the class I fructose-biphosphate aldolase family. This protein is a glycolytic enzyme that catalyzes the reversible aldol cleavage of fructose-1,6-biphosphate and fructose 1-phosphate to dihydroxyacetone phosphate and either glyceraldehyde-3-phosphate or glyceraldehydes respectively. |
Source : | E.coli |
Species : | Mouse |
Tag : | His |
Form : | Liquid, In Phosphate buffered saline (pH7.4) containing 20% glycerol, 1mM DTT |
Molecular Mass : | 41.9kDa (387aa) confirmed by MALDI-TOF |
AA Sequence : | MGSSHHHHHH SSGLVPRGSH MGSHMPHSYP ALSAEQKKEL SDIALRIVTP GKGILAADES VGSMAKRLSQ IGVENTEENR RLYRQVLFSA DDRVKKCIGG VIFFHETLYQ KDDNGVPFVR TIQDKGILVG IKVDKGVVPL AGTDGETTTQ GLDGLLERCA QYKKDGADFA KWRCVLKISD RTPSALAILE NANVLARYAS ICQQNGIVPI VEPEILPDGD HDLKRCQYVT EKVLAAVYKA LSDHHVYLEG TLLKPNMVTP GHACPIKYSP EEIAMATVTA LRRTVPPAVP GVTFLSGGQS EEEASLNLNA INRCPLPRPW ALTFSYGRAL QASALNAWRG QRDNAGAATE EFIKRAEMNG LAAQGRYEGS GDGGAAAQSL YIANHAY |
Purity : | >95% by SDS - PAGE |
Storage : | Can be stored at +4C short term (1-2 weeks). For long term storage, aliquot and store at -20C or -70C. Avoid repeated freezing and thawing cycles. |
Concentration : | 1mg/ml (determined by Bradford assay) |
Gene Name : | Aldoc aldolase C, fructose-bisphosphate [ Mus musculus ] |
Official Symbol : | Aldoc |
Synonyms : | ALDOC; aldolase C, fructose-bisphosphate; fructose-bisphosphate aldolase C; zebrin II; brain-type aldolase; aldolase 3, C isoform; scrapie responsive gene 2; scrapie-responsive protein 2; Aldo3; Scrg2; AI847350; AU040929; |
Gene ID : | 11676 |
mRNA Refseq : | NM_009657 |
Protein Refseq : | NP_033787 |
Pathway : | Fructose and mannose metabolism, organism-specific biosystem; Fructose and mannose metabolism, conserved biosystem; Gluconeogenesis, organism-specific biosystem; Gluconeogenesis, oxaloacetate =>fructose-6P, organism-specific biosystem; Gluconeogenesis, oxaloacetate => fructose-6P, conserved biosystem; |
Function : | catalytic activity; cytoskeletal protein binding; fructose-bisphosphate aldolase activity; fructose-bisphosphate aldolase activity; lyase activity; |
Products Types
◆ Recombinant Protein | ||
Aldoc-575M | Recombinant Mouse Aldoc Protein, MYC/DDK-tagged | +Inquiry |
ALDOC-317H | Recombinant Human ALDOC Protein, His (Fc)-Avi-tagged | +Inquiry |
ALDOC-282R | Recombinant Rat ALDOC Protein, His (Fc)-Avi-tagged | +Inquiry |
ALDOC-303H | Recombinant Human ALDOC Protein, MYC/DDK-tagged | +Inquiry |
ALDOC-304H | Recombinant Human ALDOC Protein, His-tagged | +Inquiry |
◆ Lysates | ||
ALDOC-8910HCL | Recombinant Human ALDOC 293 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.
Inquiry
- Reviews
- Q&As
Customer Reviews (4)
Write a reviewThe ALDOC Protein consistently produces well-defined and interpretable structural data, enabling me to unravel complex macromolecular assemblies and their mechanisms.
It reliably and accurately detects and quantifies target molecules, allowing for precise measurement of analytes in my samples.
The sensitivity and specificity of the ALDOC Protein have consistently delivered robust and consistent results, enhancing the efficiency and accuracy of my experimental workflows.
I highly recommend the ALDOC Protein for its outstanding performance in ELISA assays.
Q&As (21)
Ask a questionYes, ALDOC expression or activity can be influenced by various environmental factors. For example, changes in glucose availability and insulin signaling can modulate ALDOC expression. Additionally, oxygen levels, pH, and cellular stress can impact ALDOC activity. Environmental factors such as diet, exercise, and exposure to toxins or drugs can also affect ALDOC expression and function. These factors can potentially have implications for metabolic disorders and neurological conditions.
Currently, there are no specific drugs or compounds approved for the direct modulation of ALDOC expression or activity. However, certain compounds like dimethyl sulfoxide (DMSO) and valproic acid have been shown to increase ALDOC expression in certain cellular models. Additionally, some agents targeting glucose metabolism and glycolysis pathways might indirectly affect ALDOC activity. Nonetheless, further research is needed to identify more specific drug targets and develop therapeutic strategies involving ALDOC modulation.
While aldolase C deficiency and brain tumors are the primary conditions associated with ALDOC mutations, there is emerging evidence linking the protein to other diseases and pathological processes. Studies have suggested potential roles of ALDOC in neurodegenerative disorders, including Alzheimer's disease and Parkinson's disease. However, further research is needed to fully understand the implications of ALDOC in these contexts.
In addition to aldolase C deficiency, mutations in the ALDOC gene have been implicated in other conditions, such as brain tumors. Research suggests that alterations in ALDOC expression and activity may play a role in tumor development and progression.
The ALDOC protein plays a crucial role in brain development and function by participating in glucose metabolism and energy production. It is highly expressed in neurons and astrocytes, where it facilitates the production of ATP through glycolysis. This energy is necessary for various cellular processes, including neuronal signaling, synaptic transmission, and overall brain function. ALDOC deficiency or dysfunction can disrupt energy metabolism in the brain and have detrimental effects on brain development and function.
Currently, there are no specific drugs or therapies targeting the ALDOC protein. However, ongoing research into the biochemical and functional aspects of ALDOC may uncover new potential therapeutic strategies. For example, targeting the glycolytic pathway or modulating ALDOC expression could be areas of investigation in the future.
Mutations in the ALDOC gene can lead to a condition called aldolase C deficiency. This rare condition can cause a range of neurological symptoms, including motor dysfunction, cognitive impairment, and seizures.
The regulation of ALDOC protein expression and activity can be affected by various factors, including cellular signaling pathways, transcription factors, and post-translational modifications. For example, glucose levels and insulin signaling can influence ALDOC expression. Additionally, phosphorylation and glycosylation events can modify the activity of the protein.
Targeting ALDOC for therapeutic interventions in neurological disorders is an area of ongoing research. Modulating ALDOC expression or activity may offer potential therapeutic benefits. For example, increasing ALDOC expression or activity could enhance energy metabolism and protect against neurodegeneration in conditions like Alzheimer's or Parkinson's disease.
There is ongoing research into the potential use of ALDOC as a biomarker for certain diseases. For example, altered ALDOC expression has been observed in brain tumors and could potentially serve as a diagnostic or prognostic marker. However, more studies are needed to validate its clinical utility and determine its reliability as a biomarker.
Yes, mutations in the ALDOC gene can be inherited. Aldolase C deficiency, caused by ALDOC mutations, follows an autosomal recessive pattern of inheritance. This means that an affected individual must inherit two copies of the mutated gene (one from each parent) in order to exhibit symptoms of the disorder. If both parents carry a single copy of the mutated ALDOC gene, they have a 25% chance of having an affected child with aldolase C deficiency.
While the ALDOC protein is most well-known for its role in brain metabolism, it is also found in other tissues and organs. In non-brain tissues, ALDOC participates in the glycolytic pathway and contributes to energy production. However, the specific physiological functions of ALDOC in non-brain tissues are not as extensively studied as those in the brain.
Yes, prenatal testing is available for aldolase C deficiency. It involves analyzing fetal DNA obtained through procedures like chorionic villus sampling (CVS) or amniocentesis to identify mutations in the ALDOC gene. This allows for early detection of the condition, aiding in family planning and preparation for managing the condition after birth.
Yes, mutations in the ALDOC gene can cause a rare genetic disorder called aldolase C deficiency. This disorder is characterized by a lack or reduced activity of the ALDOC enzyme, leading to impaired glycolysis in the brain. Aldolase C deficiency can result in developmental delays, intellectual disability, abnormal muscle tone, and movement disorders
As of the latest information, there are no ongoing clinical trials specifically investigating the role of ALDOC in neurological disorders. However, research on ALDOC and its potential implications in various neurological conditions is an active area of study. It is possible that future clinical trials may emerge to explore the therapeutic potential of modulating ALDOC in specific neurological disorders.
Mutations in the ALDOC gene can be detected through genetic testing methods. DNA sequencing techniques can identify specific changes or variations in the DNA sequence of the gene, allowing for the diagnosis of aldolase C deficiency or other related conditions.
Currently, there is no specific treatment for aldolase C deficiency. Management typically focuses on supportive care and symptom relief. Physiotherapy, speech therapy, and occupational therapy may be employed to address the neurological symptoms associated with the condition.
Yes, there are ongoing studies and research related to the ALDOC protein. Scientists are aiming to further elucidate the role of ALDOC in brain development, neurological disorders, and tumor biology. Additionally, efforts are being made to understand the regulatory mechanisms involved in ALDOC expression and activity.
There is emerging evidence suggesting that altered ALDOC expression or activity may contribute to the development and progression of neurological disorders. For example, decreased ALDOC expression has been associated with Alzheimer's disease and Parkinson's disease. Additionally, changes in ALDOC expression have been observed in epilepsy, schizophrenia, and traumatic brain injury. However, the exact mechanisms by which ALDOC alterations contribute to these disorders are still not fully understood and require further investigation.
Yes, aldolase C deficiency is an inherited disorder. It follows an autosomal recessive inheritance pattern, which means that an affected individual needs to inherit two copies of the mutated ALDOC gene (one from each parent) to develop the condition.
The exact mechanisms regulating ALDOC expression in the brain are not fully understood. However, several factors and signaling pathways have been implicated in its regulation. Glucose availability and insulin signaling can influence ALDOC expression, with high glucose levels and insulin promoting its expression.
Ask a Question for All Aldoc Products
Required fields are marked with *
My Review for All Aldoc Products
Required fields are marked with *
Inquiry Basket