Recombinant Mouse ALG10B Protein

• Cat.No.: ALG10B-1541M
• Product Overview: Recombinant Mouse ALG10B full length or partial length protein was expressed.

Specification

• 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 Information

• Gene Name: Alg10b asparagine-linked glycosylation 10B (alpha-1,2-glucosyltransferase) [ Mus musculus ]
• Official Symbol: ALG10B
• Gene ID: 380959
• mRNA Refseq: NM_001033441.3
• Protein Refseq: NP_001028613.1
• UniProt ID: Q3UGP8

Reviews

07/15/2022

The protein has strong specificity.

01/08/2022

ELISA is the most suitable detection method.

08/18/2020

Compared with other methodologies, qPCR was used for detection

Q&As

Does ALG10B test require special preparation and precautions?

The testing does not require special preparation, but if a blood sample is taken, it needs to be done under the guidance of a doctor.

Does ALG10B test require fasting?

This protein testing does not require fasting.

What diseases is the ALG10B test mainly used to detect?

ALG10B detection is mainly used to detect congenital N-glycosylated striate myopathy and other related diseases.

What is the role of ALG10B in the human body?

ALG10B is an important gene involved in protein glycosylation in human body, and plays an important role in maintaining the normal function of human body.

What are the symptoms of ALG10B deficiency?

Deficiency may lead to congenital N-glycosylated striate myopathy, which is manifested by movement and respiratory disorders, intellectual impairment and other symptoms.

How is ALG10B defect caused?

ALG10B deficiency may be caused by gene mutation, loss or deletion, which in turn affects the metabolism of protein glycosylation.

What is the cost of ALG10B testing?

The cost of ALG10B testing may vary due to different hospital and regional charges.

Are there any factors that interfere with ALG10B detection?

Detection may be interfered with by a number of factors, such as clinical presentation, age, gender, diet, etc.

Does the ALG10B test require a professional?

The testing is performed by a professional clinical geneticist and laboratory technician.

What diseases can ALG10B defect cause?

ALG10B deficiency may cause congenital N-glycosylated striate myopathy, resulting in movement and breathing disorders, intellectual impairment and other symptoms.

How to interpret the test results of ALG10B?

ALG10B test results need to be interpreted and analyzed by a professional.

Does ALG10B defect affect fertility?

The defects may affect fertility and can cause problems such as genetic disorders.

How to treat ALG10B defects?

The deficiency can be treated with targeted treatment for its clinical manifestations, such as symptom relief, rehabilitation, etc.

Is ALG10B deficiency a familial genetic risk?

The deficiency has a familial genetic risk, and the risk of developing the disease depends on the family genetic history.

What groups of people are more susceptible to ALG10B defects?

ALG10B deficiency is a genetic disorder, so it may affect members of its family.

Can ALG10B test protect against disease?

ALG10B testing may help in the early detection of related diseases, so that targeted prevention and treatment measures can be taken, but often cannot prevent all related diseases.

Is ALG10B tested routinely?

This potein testing is not a routine examination procedure and is usually performed on the advice of a doctor.

Can ALG10B defects be inherited?

ALG10B deficiency is a genetic disorder that can be passed on to future generations through genes.

What is ALG10B tested for?

ALG10B is tested on samples including blood, oral swabs, etc.