ALG10B
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Official Full Name
asparagine-linked glycosylation 10B (alpha-1,2-glucosyltransferase)
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Synonyms
Gm917; C85569; AA469671; AU045404; AW123895;
- Recombinant Proteins
- Protein Pre-coupled Magnetic Beads
- Human
- Mouse
- HEK293
- Mammalian Cell
- His
- His (Fc)
- Avi
| Species | Cat.# | Product name | Source (Host) | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| Human | ALG10B-1274H | Recombinant Human ALG10B | Mammalian Cell | His |
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| Human | ALG10B-2455H | Recombinant Human ALG10B Protein, His (Fc)-Avi-tagged | HEK293 | His (Fc)-Avi |
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| Human | ALG10B-2455H-B | Recombinant Human ALG10B Protein Pre-coupled Magnetic Beads | HEK293 |
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| Mouse | ALG10B-1541M | Recombinant Mouse ALG10B Protein | Mammalian Cell | His |
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| Mouse | ALG10B-462M-B | Recombinant Mouse ALG10B Protein Pre-coupled Magnetic Beads | HEK293 |
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| Mouse | ALG10B-462M | Recombinant Mouse ALG10B Protein, His (Fc)-Avi-tagged | HEK293 | His (Fc)-Avi |
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- Involved Pathway
- Protein Function
- Interacting Protein
ALG10B involved in several pathways and played different roles in them. We selected most pathways ALG10B participated on our site, such as Asparagine N-linked glycosylation, Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein, Metabolic pathways, which may be useful for your reference. Also, other proteins which involved in the same pathway with ALG10B were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|---|
| Asparagine N-linked glycosylation | LMAN2;MGAT4A;ALG14;GOLGA2;ALG2;MIA3;PREB;ANKRD28;TRAPPC10 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | GNE;ALG2;ZNF408;MPDU1B;ST8SIA3;SLC35A1;ALG14;ST3GAL3A;NANP |
| Metabolic pathways | GCNT4A;NDUFA4L2;FTCD;ITGB1BP3;COQ6;GALNTL2;AMY2A2;UPB1;NME3 |
| Metabolism of proteins | IGF2B;ATPBD4;ARSI;TIMM23;EIF4H;EEF1B2;ARSF;FBXL5;IGFBP6A |
| N-Glycan biosynthesis | STT3A;ST6GAL2;B4GALT1;ALG3;ALG6;ALG13;DOLK;ALG5;DOLPP1 |
| Post-translational protein modification | EID3;ARSH;GALNT6;GALNTL5;TRAPPC3;SMC6;MUC15;SCMH1;TRAPPC6A |
ALG10B has several biochemical functions, for example, dolichyl-phosphate-glucose-glycolipid alpha-glucosyltransferase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by ALG10B itself. We selected most functions ALG10B had, and list some proteins which have the same functions with ALG10B. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| dolichyl-phosphate-glucose-glycolipid alpha-glucosyltransferase activity | B3GNT8;UGGT1;4931440L10Rik;PIGB;POMGNT2;GALNT18A;GALNTL4;B3GNT9-PS;GLT8D1 |
ALG10B has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with ALG10B here. Most of them are supplied by our site. Hope this information will be useful for your research of ALG10B.
- Q&As
- Reviews
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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