Recombinant Human ALG10B Protein, His (Fc)-Avi-tagged
Cat.No. : | ALG10B-2455H |
Product Overview : | Recombinant Human ALG10B with His (Fc)-Avi tag was expressed and purified |
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Source : | HEK293 |
Species : | Human |
Tag : | His (Fc)-Avi |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method |
Purity : | ≥85% by SDS-PAGE |
Stability : | Stable for at least 6 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Storage : | For long term storage, aliquot and store at -20 to -80 centigrade. Avoid repeated freezing and thawing cycles. |
Storage Buffer : | PBS buffer |
Gene Name : | ALG10B asparagine-linked glycosylation 10, alpha-1,2-glucosyltransferase homolog B (yeast) [ Homo sapiens ] |
Official Symbol : | ALG10B |
Gene ID : | 144245 |
mRNA Refseq : | NM_001013620.3 |
Protein Refseq : | NP_001013642.1 |
UniProt ID : | Q5I7T1 |
Products Types
◆ Recombinant Protein | ||
ALG10B-462M | Recombinant Mouse ALG10B Protein, His (Fc)-Avi-tagged | +Inquiry |
ALG10B-1274H | Recombinant Human ALG10B | +Inquiry |
ALG10B-1541M | Recombinant Mouse ALG10B Protein | +Inquiry |
Related Gene
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 (19)
Ask a questionThe testing does not require special preparation, but if a blood sample is taken, it needs to be done under the guidance of a doctor.
This protein testing does not require fasting.
ALG10B detection is mainly used to detect congenital N-glycosylated striate myopathy and other related diseases.
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.
Deficiency may lead to congenital N-glycosylated striate myopathy, which is manifested by movement and respiratory disorders, intellectual impairment and other symptoms.
ALG10B deficiency may be caused by gene mutation, loss or deletion, which in turn affects the metabolism of protein glycosylation.
The cost of ALG10B testing may vary due to different hospital and regional charges.
Detection may be interfered with by a number of factors, such as clinical presentation, age, gender, diet, etc.
The testing is performed by a professional clinical geneticist and laboratory technician.
ALG10B deficiency may cause congenital N-glycosylated striate myopathy, resulting in movement and breathing disorders, intellectual impairment and other symptoms.
ALG10B test results need to be interpreted and analyzed by a professional.
The defects may affect fertility and can cause problems such as genetic disorders.
The deficiency can be treated with targeted treatment for its clinical manifestations, such as symptom relief, rehabilitation, etc.
The deficiency has a familial genetic risk, and the risk of developing the disease depends on the family genetic history.
ALG10B deficiency is a genetic disorder, so it may affect members of its family.
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.
This potein testing is not a routine examination procedure and is usually performed on the advice of a doctor.
ALG10B deficiency is a genetic disorder that can be passed on to future generations through genes.
ALG10B is tested on samples including blood, oral swabs, etc.
Customer Reviews (3)
Write a reviewThe protein has strong specificity.
ELISA is the most suitable detection method.
Compared with other methodologies, qPCR was used for detection
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