Recombinant Zebrafish AP1S3B

• Cat.No.: AP1S3B-1349Z
• Product Overview: Recombinant Zebrafish AP1S3B full length or partial length protein was expressed.

Specification

• Source: Mammalian Cells
• Species: Zebrafish
• 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 Information

• Gene Name: ap1s3b adaptor-related protein complex 1, sigma 3 subunit, b [ Danio rerio (zebrafish) ]
• Official Symbol: AP1S3B
• Gene ID: 447897
• mRNA Refseq: NM_001004635
• Protein Refseq: NP_001004635
• UniProt ID: Q66IE3

Reviews

05/27/2022

Due to the short half-life and high clearance of AP1S3B, it can penetrate the tissue better and reach the lesion site, which improves the therapeutic effect.

07/26/2021

The green production process of AP1S3B not only improves the production efficiency, but also reduces the impact on the environment to the maximum, and truly realizes the win-win situation of economic and environmental benefits.

08/29/2020

The stability of AP1S3B is very strong and can maintain its structural and functional stability even after a lot of use, which shows its excellent quality and reliability.

07/17/2019

Because of its high stability, it can be widely used in various chemical reactions, and its application prospect is very broad.

Q&As

Can AP1S3B protein be used as a new tumor therapeutic target?

AP1S3B protein is related to the occurrence and progression of some tumors, and may be used as a new tumor therapeutic target, which needs further research and exploration.

What is the effect of phosphorylation of AP1S3B protein on its biological function?

Phosphorylation of the AP1S3B protein may affect its ability to bind to other proteins, thereby regulating the biological processes in which it is involved.

What are the structural characteristics of AP1S3B protein?

The AP1S3B protein is a membrane binding protein characterized by multiple alpha helix and beta folds.

How do AP1S3B mutations diagnose and treat related diseases?

Diagnosis can be made by gene sequencing, and treatment, depending on the disease, can be exogenous supplementation or gene repair.

Does AP1S3B gene participate in protein synthesis and degradation?

The AP1S3B gene has little influence on the protein synthesis and degradation process.

What is the effect of AP1S3B gene mutation on the immune system?

Certain mutations in the AP1S3B gene may lead to immune system abnormalities that trigger certain immune diseases.

What is the difference between AP1S3B and other aptamer proteins?

AP1S3B is similar to other aptamer proteins, but its more special structural characteristics and expression patterns make it exhibit unique functions in some biological processes.

How conserved is the AP1S3B gene in mammals?

The AP1S3B gene is highly conserved in mammals.

Which diseases are associated with mutations in the AP1S3B gene?

It has been reported that the mutation of AP1S3B gene is associated with some autoimmune diseases, cancer and other diseases.

Is AP1S3B involved in intracellular signal transduction?

AP1S3B protein is involved in intracellular signal transduction to some extent.

What is the expression pattern of AP1S3B protein?

AP1S3B protein is highly expressed in liver, immune cells and other tissues.

Does the AP1S3B gene participate in the localization and distribution of proteins in the cytoplasm?

AP1S3B is involved in the intracytoplasmic transport pathway, regulates the formation and transport of small vesicles, and indirectly participates in the localization and distribution of proteins in the cytoplasm.

What is the main biological function of AP1S3B protein?

The protein encoded by AP1S3B is an aptamer protein, whose main function is to participate in the intracellular transport pathway and regulate the formation and transport of small vesicles.

Is AP1S3B involved in the pathway of virus invasion?

At present, there is no relevant research to confirm it, and further research is needed.

Is AP1S3B mutation the main cause of hereditary diseases?

The AP1S3B mutation may be a cause of some genetic diseases, but it is not the main cause of all genetic diseases.

Is AP1S3B involved in the genesis and progression of tumors?

AP1S3B protein may be related to the occurrence and progression of some tumors, and the specific mechanism needs to be confirmed by further studies.

Is AP1S3B involved in nervous system development and function maintenance?

At present, there are no relevant studies to explore the relationship between AP1S3B protein and nervous system development and function maintenance.

What is the association between AP1S3B mutation and autoimmune diseases?

AP1S3B mutation is associated with certain autoimmune diseases, such as systemic lupus erythematosus and rheumatoid arthritis.

What is the relationship between AP1S3B protein and apoptosis?

AP1S3B protein is involved in regulating vesicle transport and has little effect on apoptosis.