Recombinant Mouse ADCYAP1, His-tagged, T7 tagged
Cat.No. : | ADCYAP1-3169M |
Product Overview : | Adenylate Cyclase Activating Polypeptide 1, Pituitary (ADCYAP1) |
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Description : | About the Marker: Effective Size Range: 10kDa to 70kDa.Protein bands: 10kDa, 14kDa, 18kDa, 22kDa, 26kDa, 33kDa, 44kDa and70kDa.Double intensity bands: The 26kDa, 18kDa, 10kDa bands are at doubleintensity to make location and size approximation of proteins of interestquick and easy.Ready-to-use: No need to heat, dilute or add reducing agents before use. |
Source : | E. Coli |
Species : | Mouse |
Tag : | His,T7 |
Form : | Supplied as lyophilized form in PBS,pH7.4, containing 5% sucrose, 0.01% sarcosyl. |
Molecular Mass : | 23.2kDa |
Protein length : | 175 |
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 ADCYAP1 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 : | Adcyap1 adenylate cyclase activating polypeptide 1 [ Mus musculus ] |
Official Symbol : | ADCYAP1 |
Synonyms : | ADCYAP1; adenylate cyclase activating polypeptide 1; pituitary adenylate cyclase-activating polypeptide; PACAP; |
Gene ID : | 11516 |
mRNA Refseq : | NM_009625 |
Protein Refseq : | NP_033755 |
Pathway : | Activation of TRKA receptors, organism-specific biosystem; Class B/2 (Secretin family receptors), organism-specific biosystem; G alpha (s) signalling events, organism-specific biosystem; GPCR downstream signaling, organism-specific biosystem; GPCR ligand |
Function : | hormone activity; neuropeptide hormone activity; peptide hormone receptor binding; pituitary adenylate cyclase-activating polypeptide receptor binding; receptor binding; receptor signaling protein activity; receptor signaling protein activity; |
Products Types
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ADCYAP1-333H | Recombinant Human ADCYAP1 Protein, GST-tagged | +Inquiry |
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ADCYAP1-334H | Recombinant Human ADCYAP1 Protein, GST-tagged | +Inquiry |
◆ Lysates | ||
ADCYAP1-9019HCL | Recombinant Human ADCYAP1 293 Cell Lysate | +Inquiry |
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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 (13)
Ask a questionADCYAP1 is not currently being used as a treatment for Alzheimer's disease. However, there are ongoing studies investigating the use of ADCYAP1 and its analogues as potential therapeutics for the treatment of cognitive impairment in Alzheimer's disease and other neurodegenerative disorders.
ADCYAP1 can be used as a potential therapeutic target for the treatment of inflammatory disorders. Drugs that target ADCYAP1 could potentially inhibit the production of pro-inflammatory cytokines and increase the levels of anti-inflammatory cytokines, leading to a reduction in inflammation.
ADCYAP1 can be used as a potential therapeutic target for the treatment of migraines. Drugs that target ADCYAP1 could potentially block its activity and reduce the release of neuropeptides like substance P and CGRP that are involved in migraine pain sensitization.
The potential side effects of targeting ADCYAP1 are currently unknown, as there are no drugs targeting this protein that have reached clinical trials. However, the complex regulation and interactions of ADCYAP1 with other systems, such as the immune system, may increase the risk of side effects. In addition, as ADCYAP1 plays a role in various physiological processes, targeting it may have unintended effects beyond the intended therapeutic target.
There are currently no drugs targeting ADCYAP1 that have been approved by regulatory agencies for clinical use. However, there are ongoing preclinical studies investigating the use of ADCYAP1 and its analogues as potential therapeutics for various conditions, including Alzheimer's disease, diabetes, and inflammatory disorders.
Targeting ADCYAP1 protein may have therapeutic applications in various diseases and conditions, including migraine headache, Alzheimer's disease, schizophrenia, diabetes, and inflammatory disorders.
Various approaches are being explored for targeting ADCYAP1 protein in drug development, including small molecule inhibitors, monoclonal antibodies, and gene therapy. Small molecule inhibitors that target ADCYAP1 activity or expression are being developed and tested in preclinical studies. Monoclonal antibodies that bind to ADCYAP1 or its receptors are being developed for diagnostic and therapeutic purposes. Gene therapy approaches are being explored to deliver ADCYAP1-targeted therapeutics to specific tissues.
As of 2021, there are no drugs targeting ADCYAP1 that have reached clinical trials. However, several small molecule inhibitors of ADCYAP1 are being developed by pharmaceutical companies and tested in preclinical studies.
ADCYAP1 has anti-inflammatory properties and has been shown to regulate the function of immune cells such as macrophages and T cells. It reduces inflammation by inhibiting the production of pro-inflammatory cytokines and increasing the levels of anti-inflammatory cytokines. Elevated levels of ADCYAP1 have been found in the synovial fluid of patients with rheumatoid arthritis, suggesting that it may play a role in modulating the inflammatory response in this disorder.
ADCYAP1 can be used as a potential therapeutic target for the treatment of diabetes. Drugs that target ADCYAP1 could potentially stimulate insulin release from pancreatic beta cells and enhance insulin sensitivity in peripheral tissues, leading to improved glucose homeostasis.
As ADCYAP1 is involved in various physiological processes and diseases, potential biomarkers for monitoring the efficacy of ADCYAP1-targeted therapies may depend on the disease or condition being treated. For example, in migraine headache, biomarkers such as headache frequency and severity, medication use, and neuroimaging measures may be used. In Alzheimer's disease, biomarkers such as cognitive function and neuroimaging measures may be monitored. In diabetes, biomarkers such as blood glucose levels and insulin sensitivity may be measured.
ADCYAP1 has neuroprotective properties and has been shown to improve cognitive function in animal models of Alzheimer's disease. It also regulates the production and clearance of beta-amyloid, a protein that accumulates in the brains of Alzheimer's patients and is associated with neurodegeneration. However, studies have also shown that elevated levels of ADCYAP1 in the brain may contribute to the formation of tau protein, another hallmark of Alzheimer's disease pathology.
One challenge in developing ADCYAP1-targeted therapies is that ADCYAP1 is not the only neuropeptide that plays a role in the physiological processes and diseases in which it is implicated. Its physiological effects may also depend on its interactions with other neuropeptides, receptors, and signaling pathways. Additionally, the complex regulation and interactions of ADCYAP1 with other systems, such as the immune system, may complicate the design and optimization of ADCYAP1-targeted therapeutics.
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