Recombinant Rat AP1B1 Protein

• Cat.No.: AP1B1-698R
• Product Overview: Recombinant Rat AP1B1 full length or partial length protein was expressed.

Specification

• Source: Mammalian Cells
• Species: Rat
• 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: Ap1b1 adaptor-related protein complex 1, beta 1 subunit [ Rattus norvegicus ]
• Official Symbol: AP1B1
• Gene ID: 29663
• mRNA Refseq: NM_017277.1
• Protein Refseq: NP_058973.1
• UniProt ID: P52303

Reviews

10/11/2022

Reproducibility of the AP1B1 is very good, which can reduce the error in the experiment and improve the repeatability of the experiment.

11/07/2020

AP1B1 labeling effect is very good, can be used for fluorescence labeling, etc., which is very suitable for our research.

03/30/2020

It is very stable, even after multiple uses or storage, its structure and function remain stable, providing strong support for long-term experiments and applications.

05/21/2019

Catalytic activity of this protein is very strong, which can make chemical reactions that are difficult to carry out easy to achieve, and has high application potential.

Q&As

Does AP1B1 mutation cause vision problems?

AP1B1 mutations may be associated with retinal diseases, but there are relatively few studies directly related to vision problems.

Is AP1B1 mutation associated with mental illness?

Some studies have shown that the AP1B1 gene mutation may be associated with some mental diseases such as schizophrenia.

What is the effect of AP1B1 mutation on treatment?

AP1B1 mutation may affect intracellular vesicle transport and membrane protein localization, thus affecting the efficacy of therapy and the action of drugs.

Is AP1B1 mutation related to intelligence development?

Some studies have shown that mutations in the AP1B1 gene may be associated with diseases related to intellectual development.

What diseases are associated with AP1B1 mutations?

AP1B1 mutations may be associated with a variety of diseases, including congenital retinitis pigmentosa and neurodegenerative diseases.

Can AP1B1 mutation be repaired by gene editing?

Gene-editing techniques such as CRISPR-Cas9 could potentially be used to fix AP1B1 mutations, but they are still in the laboratory stage and require further research and trials.

Can AP1B1 mutations be inherited?

AP1B1 mutation may be hereditary, and the specific inheritance pattern may be related to each specific mutation.

How to treat diseases caused by AP1B1 mutations?

There is currently no specific treatment for diseases caused by AP1B1 mutations, but the quality of life of patients can be improved through symptom relief treatment and rehabilitation training.

What is the function of AP1B1?

AP1B1 plays an important role in cell regulation by participating in intracellular vesicle transport and cell membrane protein localization.

How does AP1B1 mutation affect intracellular signaling?

AP1B1 mutation may lead to the abnormality of intracellular signal transduction pathway and affect the normal process of various biochemical reactions in the cell.

How can AP1B1 mutation be prevented?

There is currently no direct way to prevent AP1B1 mutations, but a healthy lifestyle and genetic counseling may help reduce the risk of certain genetic diseases.

What is the latest progress of AP1B1 research?

Recent studies have shown that AP1B1 plays an important role in intracellular vesicle transport and neuronal development.

Does AP1B1 mutation affect life span?

It is unclear whether AP1B1 mutations directly affect longevity.

How to detect AP1B1 gene mutation?

AP1B1 gene mutation can be detected by molecular biological methods such as gene sequencing.