Recombinant Mouse Aip Protein, MYC/DDK-tagged
Cat.No. : | Aip-559M |
Product Overview : | Purified recombinant protein of full-length mouse aryl-hydrocarbon receptor-interacting protein (Aip), with C-terminal MYC/DDK tag, expressed in HEK293T cells. |
- Specification
- Gene Information
- Related Products
Description : | This gene encodes an Hsp90-associated protein that is localized to the cytoplasm. The encoded protein interacts with the aryl hydrocarbon receptor (AhR) and the tyrosine kinase receptor RET, inhibits AhR ubiquitination, and regulates the intracellular localization of AhR. Alternative splicing results in multiple transcript variants. |
Source : | HEK293T |
Species : | Mouse |
Tag : | MYC/DDK |
Molecular Mass : | 37.6 kDa |
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 after receiving vials. |
Concentration : | >50 μg/mL as determined by microplate BCA method |
Storage Buffer : | 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol. |
Gene Name : | Aip aryl-hydrocarbon receptor-interacting protein [ Mus musculus (house mouse) ] |
Official Symbol : | Aip |
Synonyms : | Aip; aryl-hydrocarbon receptor-interacting protein; Ara9; Xap2; Fkbp16; AA408703; AW476050; D19Bwg1412e; AH receptor-interacting protein; EC 5.2.1.8 |
Gene ID : | 11632 |
mRNA Refseq : | NM_016666 |
Protein Refseq : | NP_057875 |
UniProt ID : | O08915 |
Products Types
◆ Recombinant Protein | ||
AIP-3595H | Recombinant Human AIP, His-tagged | +Inquiry |
AIP-417M | Recombinant Mouse AIP Protein, His (Fc)-Avi-tagged | +Inquiry |
AIP-109R | Recombinant Rhesus Macaque AIP Protein, His (Fc)-Avi-tagged | +Inquiry |
AIP-510H | Recombinant Human AIP Protein, His-tagged | +Inquiry |
AIP-2449H | Recombinant Human AIP Protein, His (Fc)-Avi-tagged | +Inquiry |
◆ Lysates | ||
AIP-8950HCL | Recombinant Human AIP 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.
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Q&As (13)
Ask a questionWhile there is no direct dietary link to the AIP protein, there are some dietary protocols that are known as the Autoimmune Protocol (AIP) that are designed to reduce inflammation and balance the immune system. The AIP diet is a restrictive form of the paleo diet that eliminates foods that are known to commonly cause food allergies or sensitivities, such as gluten, dairy, grains, legumes, and nightshade vegetables. The purpose of the AIP diet is to give the body a chance to heal and reduce inflammation, which may help with autoimmune conditions that are linked to AIP mutations.
Reduced expression of the AIP protein has been associated with increased risk of cancer, particularly pituitary adenomas and other endocrine tumors. It has also been suggested that reduced AIP expression may play a role in the development and progression of other types of cancer. However, more research is needed to understand the exact mechanisms involved and how the AIP protein can be targeted for cancer prevention or treatment.
Treatment for AIP-related conditions depends on the specific condition and the individual patient's needs. For pituitary adenomas or other endocrine tumors associated with AIP mutations, treatment may involve surgery, radiation therapy, chemotherapy, or medication to control hormone secretion. Patients with FIPA may undergo regular monitoring and screening to detect early signs of tumors. Hormone replacement therapy may also be necessary to manage hormone deficiencies in patients with pituitary tumors.
Yes, individuals with AIP mutations can have children if they wish to do so. However, there is a 50% chance that the mutation will be passed on to each child. Genetic counseling may be recommended for individuals with AIP mutations who are considering having children to discuss their options and the risks involved.
Currently, there is no cure for AIP-related conditions. Treatment is focused on managing symptoms, controlling hormone secretion, and removing or shrinking tumors, if necessary. Research is ongoing to identify new treatments and therapies for these conditions.
In patients with FIPA, genetic testing for mutations in the AIP gene can aid in diagnosis and guide treatment. In oncology, the AIP protein has been suggested as a potential biomarker for cancer prognosis and treatment response. Additionally, researchers are investigating the use of the AIP protein as a therapeutic target for cancer treatment.
AIP mutations are rare and only account for a small percentage of cases of pituitary adenomas and other endocrine tumors. The exact prevalence of AIP mutations in the general population is not known, but estimates suggest that they may be found in less than 1% of people with pituitary adenomas.
Yes, although AIP mutations are primarily associated with pituitary adenomas and other endocrine tumors, some individuals with AIP mutations may experience other symptoms, including headaches, fatigue, muscle weakness, joint pain, and gastrointestinal issues. These symptoms are not directly related to AIP mutations but may be associated with underlying health conditions or other factors.
Future research on the AIP protein may focus on understanding its role in cancer development and progression, as well as potential therapeutic targets for cancer treatment. Other areas of interest include the role of the AIP protein in the regulation of pituitary hormone secretion, and the potential use of the AIP protein as a diagnostic biomarker or therapeutic target for various health conditions associated with AIP mutations.
AIP mutations can be identified through genetic testing, which involves analyzing a person's DNA for known mutations in the AIP gene. Genetic testing may be recommended for individuals with a personal or family history of pituitary adenomas, other endocrine tumors, or other conditions associated with AIP mutations. Testing may also be recommended for individuals who have symptoms or signs of a hormone imbalance or other tumor-related issues.
In addition to FIPA, mutations in the AIP gene have been associated with other health conditions such as acromegaly, gigantism, and Cushing's disease. These conditions are characterized by hormonal imbalances that result in abnormal growth, particularly in the pituitary gland. AIP mutations have also been linked to increased risk of breast cancer.
Yes, AIP mutations can be inherited in an autosomal dominant manner, meaning that only one copy of the mutated gene is needed to cause the condition. This means that a person with an AIP mutation has a 50% chance of passing the mutation on to each of their children.
Currently, there are no known preventative measures for AIP-related conditions. However, genetic testing can be a useful tool for identifying individuals who may be at increased risk for developing these conditions. Regular monitoring and screening may be recommended for individuals with AIP mutations or a family history of pituitary adenomas or other endocrine tumors.
Customer Reviews (3)
Write a reviewTheir expertise and commitment to excellence guarantee swift resolution of any issues, facilitating seamless progress in my research endeavors.
By harnessing the power of the AIP protein and leveraging the manufacturer's exceptional technical assistance, my experimental obstacles can be effortlessly overcome.
With an insight into the complex mechanisms governed by AIP, this protein empowers me to unravel mysteries in my field and expands the horizon of possibilities in scientific advancement.
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