Recombinant Human ADCY2, His-tagged, T7 tagged
Cat.No. : | ADCY2-3167H |
Product Overview : | Adenylate Cyclase 2, Brain (ADCY2) |
- Specification
- Gene Information
- Related Products
Description : | This gene encodes a member of the family of adenylate cyclases, which are membrane-associated enzymes that catalyze the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). This enzyme is insensitive to Ca(2+)/calmodulin, and is stimulated by the G protein beta and gamma subunit complex. |
Source : | E. Coli |
Species : | Human |
Tag : | His,T7 |
Form : | Supplied as lyophilized form in PBS,pH7.4, containing 5% sucrose, 0.01% sarcosyl. |
Molecular Mass : | 29.8kDa |
Protein length : | 1091 |
Endotoxin : | <1.0eu per 1ug (determined by the lal</1.0eu |
Purity : | >95% |
Applications : | SDS-PAGE, Western Blot (WB), ELISA (EIA), Immunoprecipitation (IP) |
Notes : | Small volumes of ADCY2 recombinant protein may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice. |
Storage : | Avoid repeated freeze/thaw cycles. Store at 2-8 degree C for one month. Aliquot and store at -80 degree C for 12 months.Stability Test: The thermal stability is described by the loss rate of the targetprotein. The loss rate was determined by accelerated thermal degradation test,that is, incubate the protein at 37 degree C for 48h, and no obvious degradation andprecipitation were observed. (Referring from China Biological Products Standard,which was calculated by the Arrhenius equation.) The loss of this protein is lessthan 5% within the expiration date under appropriate storage condition. |
Reconstitution : | Reconstitute in sterile PBS, pH7.2-pH7.4. |
Warning : | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Gene Name : | ADCY2 adenylyl cyclase 2 [ Homo sapiens ] |
Official Symbol : | ADCY2 |
Synonyms : | ADCY2; adenylyl cyclase 2; |
Gene ID : | 254679 |
Products Types
◆ Recombinant Protein | ||
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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 (11)
Ask a questionYes, studies have suggested that ADCY2-mediated signaling may be involved in the pathogenesis of schizophrenia, and drugs that target ADCY2 activity are being developed as potential treatments for the disease. For example, a range of compounds that selectively inhibit ADCY2 activity have been identified and tested in animal models of schizophrenia, with promising results.
ADCY2 protein has been implicated in various diseases, including diabetes, hypertension, schizophrenia, and addiction. As such, it has been suggested that targeting ADCY2 protein activity could be a therapeutic approach for these conditions. For example, drugs that inhibit ADCY2 protein activity could potentially reduce insulin resistance in diabetes patients or help to mitigate the symptoms of schizophrenia.
While genetic variants in the ADCY2 gene are associated with an increased risk of type 2 diabetes, ADCY2 protein itself has not been widely studied as a diagnostic biomarker for the disease. Other biomarkers, such as blood glucose levels and insulin secretion, are currently used to diagnose type 2 diabetes.
The primary function of ADCY2 protein is to catalyze the formation of cAMP, which is a second messenger that mediates diverse cellular signaling pathways. It is involved in regulating the activity of ion channels, protein kinases, and transcription factors, which ultimately affects the function of various organ systems, including the nervous, cardiovascular, and endocrine systems.
Yes, ADCY2 protein has been identified as a potential therapeutic target for the treatment of heart failure. Studies have shown that reduced ADCY2 expression and activity are associated with impaired cardiac function, while increasing ADCY2 activity can improve cardiac function in animal models of heart failure. As such, drugs that target ADCY2 activity are being developed as potential therapies for heart failure.
ADCY2 protein can be studied in vitro using recombinant protein expression systems or in vivo using animal models. Common techniques used to study ADCY2 protein function include enzyme assays to measure cAMP production, electrophysiology to examine ion channel activity, and genetic manipulation to study the effect of altering ADCY2 gene expression.
While ADCY2 protein is not usually considered a direct target for cancer therapy, the cAMP signaling pathway in which ADCY2 participates has been targeted in some cancer treatments. For example, drugs that activate ADCY2 by increasing cAMP levels have been tested as potential therapies for some types of cancer, including colon cancer and melanoma. Additionally, several other components of the cAMP signaling pathway are known to be important in cancer growth and progression, and drugs that target these proteins are being developed as potential cancer treatments.
At present, there are no FDA-approved drugs that specifically target ADCY2 protein. However, several compounds have been identified that can modulate the activity of adenylate cyclases, including ADCY2. For example, forskolin, which stimulates adenylate cyclase activity, is commonly used as a research tool to increase intracellular cAMP levels. In addition, several drugs that target other components of the cAMP signaling pathway, such as phosphodiesterase inhibitors, have been developed and are used clinically.
Yes, mutations in the ADCY2 gene have been associated with several diseases. For example, a single nucleotide polymorphism (SNP) in the ADCY2 gene has been linked to an increased risk of type 2 diabetes. In addition, mutations in ADCY2 have been associated with familial cases of schizophrenia and bipolar disorder.
While mutations in the ADCY2 gene have been associated with an increased risk of primary open-angle glaucoma, ADCY2 protein itself has not been widely studied as a potential diagnostic biomarker for the disease. Other biomarkers, such as intraocular pressure and optic nerve head anatomy, are currently used to diagnose primary open-angle glaucoma.
ADCY2 protein activity is regulated by several mechanisms. For example, it can be stimulated by G protein-coupled receptors (GPCRs) that activate adenylate cyclase via a G protein-dependent pathway. Other factors that can stimulate ADCY2 protein activity include calcium/calmodulin and forskolin. In addition, the activity of ADCY2 protein can be inhibited by protein kinase A (PKA), which phosphorylates ADCY2 and reduces its activity. Genetic mutations and epigenetic modifications, such as DNA methylation, can also affect the expression and activity of ADCY2 protein.
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