Recombinant Rat ALG10 Protein
Cat.No. : | ALG10-627R |
Product Overview : | Recombinant Rat ALG10 full length or partial length protein was expressed. |
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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 Name : | Alg10 asparagine-linked glycosylation 10, alpha-1,2-glucosyltransferase homolog (S. pombe) [ Rattus norvegicus ] |
Official Symbol : | ALG10 |
Gene ID : | 245960 |
mRNA Refseq : | NM_139101.2 |
Protein Refseq : | NP_620801.1 |
MIM : | |
UniProt ID : | O88788 |
Products Types
◆ Recombinant Protein | ||
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ALG10-460H | Recombinant Human ALG10 Protein, GST-tagged | +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 questionDefects may affect fertility and can cause problems such as genetic disorders.
ALG10 testing does not require fasting.
Defects are usually caused by mutations, loss or deletion of genes, which in turn affect the metabolism of protein glycosylation.
ALG10 is an important gene involved in protein glycosylation in human body and plays an important role in maintaining the normal function of human body.
ALG10 detection is mainly used to detect CDG-Ii and other related diseases.
The cost of ALG10 testing will vary due to different hospital and regional charges.
ALG10 deficiency has a familial genetic risk, and the risk of developing the disease depends on the family genetic history.
ALG10 detection can be interfered with by a number of factors, such as clinical symptoms, age, gender, diet, and so on.
This protein test results need to be interpreted and analyzed by a professional.
Testing needs to be performed by a professional clinical geneticist and laboratory technician.
ALG10 defects may cause CDG-Ii symptoms, including developmental delays, typical facial features, and low height.
ALG10 deficiency can be treated with targeted treatment for its clinical manifestations, such as symptom relief, rehabilitation, etc.
ALG10 defects can lead to the rare disease CDG-Ii, with symptoms including developmental delays, typical facial features, and low height.
ALG10 deficiency is a genetic disorder that can be passed on to future generations through genes.
ALG10 can be tested in the form of blood or oral swabs.
Testing does not require special preparation, but if a blood sample needs to be collected, the blood collection process needs to be completed under the guidance of a doctor.
The 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.
ALG10 deficiency is a genetic disorder, so it may affect members of its family.
ALG10 testing is not a routine examination procedure and is usually done on the advice of a doctor.
Customer Reviews (4)
Write a reviewStrong reducibility.
Low requirements on storage environment.
Selective for strong cofactors of NADP(H).
At the same dose, the protein was highly expressed.
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