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Recombinant Mouse AKAP17B Protein

Cat.No. : AKAP17B-1475M
Product Overview : Recombinant Mouse AKAP17B full length or partial length protein was expressed.
  • Specification
  • Gene Information
  • Related Products
Source : Mammalian Cells
Species : Mouse
Tag : His
Form : Liquid or lyophilized powder
Endotoxin : < 1.0 EU per μg of the protein as determined by the LAL method.
Purity : >80%
Notes : This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
Storage : Store it at +4 ºC for short term. For long term storage, store it at -20 ºC~-80 ºC.
Storage Buffer : PBS buffer
Gene Name : Akap17b A kinase (PRKA) anchor protein 17B [ Mus musculus ]
Official Symbol : AKAP17B
Gene ID : 338351
mRNA Refseq : NM_001081956.1
Protein Refseq : NP_001075425.1
MIM :
UniProt ID : A2A3V1

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 (16)

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Is AKAP17B expressed in specific tissues or cell types? 05/09/2023

The tissue and cell type-specific expression pattern of AKAP17B has not been extensively characterized. However, data from publicly available gene expression databases suggest that AKAP17B is expressed in various tissues, including the brain, heart, and testis. Further studies, such as RNA expression profiling, would provide more detailed information about the specific tissues and cell types in which AKAP17B is expressed.

Are there any known genetic alterations or mutations in AKAP17B? 02/05/2023

As of now, there is limited information on genetic alterations or mutations in AKAP17B. However, genetic variations, such as single nucleotide polymorphisms (SNPs), can occur within AKAP genes and potentially impact their function. It is possible that similar genetic alterations or mutations can occur in AKAP17B, but further research is needed to determine the prevalence and functional consequences of these alterations.

Has AKAP17B been implicated in cancer progression? 10/19/2022

There is currently no evidence suggesting a direct involvement of AKAP17B in cancer progression. However, the dysregulation of PKA signaling pathways, which AKAP17B may be involved in, has been linked to various types of cancer. It is worth exploring whether AKAP17B or related signaling pathways have any impact on cancer biology, but more research is necessary to establish any direct associations.

What are the structural features of AKAP17B? 04/22/2022

The structural features of AKAP17B have not been extensively characterized. AKAPs typically contain multiple protein-protein interaction domains, such as an amphipathic helix (AH) domain and one or more PKA-binding domains (PKA-BDs). These domains allow AKAPs to interact with PKA and other signaling molecules. Further research, such as structural studies or domain mapping experiments, would be necessary to elucidate the structural features and domain organization of AKAP17B.

Are there any known interacting partners of AKAP17B? 04/13/2022

Currently, there is limited information available regarding the specific interacting partners of AKAP17B. Further experimental studies, such as protein-protein interaction assays, are needed to identify potential binding partners and elucidate the molecular networks in which AKAP17B may be involved.

Does AKAP17B play a role in cellular signaling pathways? 03/15/2022

The specific role of AKAP17B in cellular signaling pathways is not yet well understood. However, AKAPs in general are known to play crucial roles in organizing and directing signaling events by scaffolding various signaling molecules.

Are there any known genetic variants or mutations in AKAP17B? 02/06/2022

Currently, there is limited information available regarding genetic variants or mutations in AKAP17B. It would be important to investigate the presence of any sequence variations in the AKAP17B gene across individuals or disease cohorts to determine if such variants may be associated with specific phenotypes or diseases.

Are there any known phosphorylation sites on AKAP17B? 03/26/2021

Currently, there is limited information available regarding the phosphorylation sites on AKAP17B. Phosphorylation of a protein is a common post-translational modification that can regulate protein function and interactions. Further experimental studies, such as phosphoproteomic analyses or site-directed mutagenesis, would be required to identify and characterize potential phosphorylation sites on AKAP17B.

Can AKAP17B be regulated by post-translational modifications? 05/17/2020

The post-translational modifications of AKAP17B have not been extensively studied. However, like many proteins, AKAP17B could potentially undergo various modifications, including phosphorylation, acetylation, or ubiquitination, which might regulate its function and activity. Future research is needed to ascertain the specific post-translational modifications that AKAP17B may undergo and their functional consequences.

Is AKAP17B involved in neuronal signaling? 08/14/2019

The involvement of AKAP17B in neuronal signaling has not been extensively studied. However, as an AKAP protein, it is possible that AKAP17B may have a role in regulating PKA-mediated signaling pathways in neurons. Further research is necessary to investigate its specific involvement in neuronal signaling processes.

Can AKAP17B interact with other AKAPs or form protein complexes? 07/28/2018

The interaction of AKAP17B with other AKAPs or its ability to form protein complexes has not been well documented. However, AKAPs in general are known to participate in dynamic protein-protein interactions and the formation of multi-protein complexes. Therefore, it is possible that AKAP17B may interact with other AKAPs or proteins to regulate signaling pathways, but further experimental studies are needed to confirm this.

Is there evidence for any post-translational modifications of AKAP17B? 03/28/2018

As of now, there is no specific evidence for post-translational modifications of AKAP17B. However, AKAPs in general can be subject to various post-translational modifications, including phosphorylation, acetylation, ubiquitination, and sumoylation. These modifications can regulate the function, localization, or stability of AKAP proteins. Further research is needed to determine if AKAP17B undergoes post-translational modifications and the functional consequences of those modifications.

Is there any information on the cellular localization of AKAP17B? 09/08/2017

The specific cellular localization of AKAP17B has not been extensively characterized. However, studies have reported that AKAP17B is targeted to the centrioles during mitosis and is involved in regulating the formation and function of the mitotic spindle. Additional research is needed to determine the precise subcellular localization of AKAP17B and its potential roles in other cellular compartments.

Are there any known isoforms or splice variants of AKAP17B? 02/01/2017

Currently, there is limited information available on the isoforms or splice variants of AKAP17B. Further research is needed to explore the existence and potential functional differences of any isoforms or splice variants of this protein.

What are the known domains within AKAP17B? 12/08/2015

AKAP17B is predicted to contain an AKAP domain, which is responsible for interacting with PKA and anchoring it to specific subcellular locations. The presence of this domain suggests that AKAP17B may function as a scaffolding protein in PKA-mediated signaling pathways.

Are there any diseases or disorders associated with AKAP17B? 02/15/2015

The specific involvement of AKAP17B in diseases or disorders is not well understood. However, dysregulation of PKA signaling pathways, in which AKAP17B may be involved, has been implicated in various diseases, including cardiovascular diseases, neurological disorders, and cancer. It would be interesting to determine if AKAP17B has any direct associations with specific diseases or disorders through its role in these signaling pathways, but further investigation is needed.

Customer Reviews (4)

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Reviews
04/03/2022

    I am sincerely grateful for the availability of such a high-quality product, as it undoubtedly contributes to the advancement of my scientific pursuits.

    10/03/2021

      The manufacturer's commitment to delivering exceptional customer support greatly enhances my research experience and provides peace of mind throughout the scientific process.

      01/18/2019

        the manufacturer offers excellent technical support that has proven to be invaluable in solving any challenges I may encounter.

        12/31/2018

          Their team of dedicated experts is readily available to address any queries or concerns, offering timely and effective solutions to ensure smooth progress in my experiments.

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