Recombinant Zebrafish ADOA

• Cat.No.: ADOA-1923Z
• Product Overview: Recombinant Zebrafish ADOA 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: adoa 2-aminoethanethiol (cysteamine) dioxygenase a [ Danio rerio (zebrafish) ]
• Official Symbol: ADOA
• Gene ID: 494091
• mRNA Refseq: NM_001008634
• Protein Refseq: NP_001008634
• UniProt ID: Q5PRD3

Reviews

08/27/2022

The purity and consistency of the protein are impressive, and I believe they will enable me to obtain reliable and reproducible results.

04/03/2021

I am confident that with this protein and the manufacturer's assistance, I will achieve the results I need.

08/16/2020

the manufacturer's technical support team has been extremely knowledgeable and responsive.

07/27/2017

I have already had great success using this protein in preliminary experiments, and I am confident that it will perform just as well in larger-scale experiments.

Q&As

Can ADOA lead to other health problems?

ADOA is primarily associated with vision loss, but some individuals with the condition may also experience hearing loss, balance problems, or muscle weakness.

How is ADOA diagnosed?

ADOA is typically diagnosed through a combination of a clinical exam, family history, and genetic testing.

How is ADOA diagnosed?

ADOA is typically diagnosed through a comprehensive eye exam that includes tests to assess visual acuity, visual field, and color vision. Additional tests such as optical coherence tomography (OCT), visual evoked potential (VEP), and genetic testing may also be done to confirm the diagnosis.

Are there any support groups or resources available for individuals living with ADOA or their families?

Yes, there are several support groups and resources available for individuals living with ADOA or their families. These groups can provide emotional support, information about the condition, and connections to medical experts and researchers specializing in ADOA.

Are there any clinical trials available for ADOA?

Yes, there are clinical trials available for ADOA. These trials aim to develop new treatments for the condition and improve our understanding of the disease.

How is ADOA treated?

Currently, there is no cure for ADOA. However, the symptoms can be managed and the progression of vision loss can be slowed down with appropriate treatment. Treatment options include visual aids such as glasses, contact lenses, and magnifying devices, low vision rehabilitation, and genetic counseling. Additionally, there are ongoing research studies to develop new treatments for ADOA, including gene therapies and drug treatments.

Can ADOA be prevented?

As ADOA is a genetic condition, it cannot be prevented. However, genetic counseling can help individuals and families make informed decisions about family planning and manage the risk of passing on the genetic mutation to future generations.

What are the common symptoms of ADOA?

The common symptoms of ADOA include progressive vision loss, usually starting with peripheral vision and progressing to central vision, and color vision impairment. Other less common symptoms may include optic nerve pallor, nystagmus, and visual field defects.

Is ADOA a hereditary condition?

Yes, ADOA is a hereditary condition that is passed down from parents to their children.

Is genetic counseling recommended for individuals with ADOA or those at risk of developing the condition?

Yes, genetic counseling is recommended for individuals with ADOA or those at risk of developing the condition. This counseling can provide information about the risk of passing on the genetic mutation to children and offer guidance on family planning and possible treatment options.

Is research currently being conducted on ADOA?

Yes, there is ongoing research into ADOA, with the goal of developing better treatments and eventually a cure for the condition.

How are ADOA proteins related to ADOA?

ADOA proteins are the proteins that are affected by the genetic mutation that causes ADOA.

Can lifestyle changes or dietary modifications help manage ADOA symptoms?

There is currently no scientific evidence that lifestyle changes or dietary modifications can manage ADOA symptoms. However, maintaining a healthy lifestyle can help manage other health conditions or complications that may arise due to ADOA.

What are some of the symptoms of ADOA?

Some of the symptoms of ADOA include vision loss or blindness, color vision defects, and optic nerve pallor.