Recombinant Mouse Alg1 Protein, Myc/DDK-tagged
Cat.No. : | Alg1-1597M |
Product Overview : | Purified recombinant protein of mouse full-length asparagine-linked glycosylation 1 (beta-1,4-mannosyltransferase) (Alg1), with C-terminal MYC/DDK tag, expressed in HEK293T cells. |
- Specification
- Gene Information
- Related Products
Description : | Participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. Involved in assembling the dolichol-pyrophosphate-GlcNAc2-Man5 intermediate on the cytoplasmic surface of the ER. |
Source : | HEK293T |
Species : | Mouse |
Tag : | Myc/DDK |
Molecular Mass : | 54.9 kDa |
Purity : | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Stability : | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Storage : | Store at -80 centigrade after receiving vials. |
Concentration : | >50 μg/mL as determined by microplate BCA method |
Storage Buffer : | 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol. |
Gene Name : | Alg1 asparagine-linked glycosylation 1 (beta-1,4-mannosyltransferase) [ Mus musculus (house mouse) ] |
Official Symbol : | Alg1 |
Synonyms : | ALG1; asparagine-linked glycosylation 1 homolog (yeast, beta-1,4-mannosyltransferase); chitobiosyldiphosphodolichol beta-mannosyltransferase; beta-1,4 mannosyltransferase; beta-1,4-mannosyltransferase; GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase; asparagine-linked glycosylation protein 1 homolog; GDP-mannose-dolichol diphosphochitobiose mannosyltransferase; HMT1; HMAT1; MGC18946 |
Gene ID : | 208211 |
mRNA Refseq : | NM_145362 |
Protein Refseq : | NP_663337 |
UniProt ID : | Q921Q3 |
Products Types
◆ Recombinant Protein | ||
ALG1-2454H | Recombinant Human ALG1 Protein, His (Fc)-Avi-tagged | +Inquiry |
ALG1-461M | Recombinant Mouse ALG1 Protein, His (Fc)-Avi-tagged | +Inquiry |
ALG1-771H | Recombinant Human ALG1 | +Inquiry |
ALG1-459H | Recombinant Human ALG1 Protein, GST-tagged | +Inquiry |
ALG1-10240Z | Recombinant Zebrafish ALG1 | +Inquiry |
◆ Lysates | ||
ALG1-8909HCL | Recombinant Human ALG1 293 Cell Lysate | +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.
Inquiry
- Q&As
- Reviews
Q&As (19)
Ask a questionALG1 testing costs vary by hospital and region and may fluctuate within a range.
ALG1 testing does not require special preparation before it is performed, but if a blood sample needs to be collected, the blood collection process needs to be completed under the guidance of a doctor.
ALG1 deficiency is a genetic disorder, so it may affect members of its family.
ALG1 defects are usually caused by mutations, loss or deletion of genes, which in turn affect the metabolism of protein glycosylation.
ALG1 defects may affect fertility and can cause problems such as genetic disorders.
ALG1 is an important gene involved in protein glycosylation in human body, and plays an important role in maintaining the normal function of human body.
Testing is not a routine procedure and is usually done on the advice of a doctor.
Detection can be interfered with by a number of factors, such as clinical symptoms, age, gender, diet, and so on.
Deficiency has a familial genetic risk, and the risk of developing the disease depends on the family genetic history.
ALG1 test results need to be interpreted and analyzed by a professional.
ALG1 testing is performed by a professional clinical geneticist and laboratory technician.
ALG1 detection is mainly used to detect CDG1K and other related diseases.
ALG1 deficiency is a genetic disorder that can be passed on to future generations through genes.
This protein can be tested in the form of blood or oral swabs.
Testing does not require fasting.
Deficiency of ALG1 may cause a rare glycoprotein Disorder called Glycosylation 1k syndrome (CDG1K), which includes mental retardation, motor degeneration, and muscle relaxation.
Deficiency may cause mental retardation, motor function degradation, fluid on the head, eye problems and other symptoms.
Deficiency can be treated with targeted treatment for its clinical manifestations, such as symptom relief, rehabilitation, etc.
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.
Customer Reviews (4)
Write a reviewThe protein specificity is high and the misdiagnosis rate is low.
The most suitable detection method is ELISA.
High sensitivity in diagnosis.
Detection limit is low, low content can also be successfully detected。
Ask a Question for All Alg1 Products
Required fields are marked with *
My Review for All Alg1 Products
Required fields are marked with *
Inquiry Basket