Recombinant Full Length Dictyostelium Discoideum Chitobiosyldiphosphodolichol Beta-Mannosyltransferase(Alg1) Protein, His-Tagged
Cat.No. : | RFL-7530DF |
Product Overview : | Recombinant Full Length Dictyostelium discoideum Chitobiosyldiphosphodolichol beta-mannosyltransferase(alg1) Protein (P90522) (1-493aa), fused to N-terminal His tag, was expressed in E. coli. |
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Source : | E.coli expression system |
Species : | Dictyostelium discoideum (Slime mold) |
Tag : | His |
Form : | Lyophilized powder |
Protein length : | Full Length (1-493) |
AA Sequence : | MNRVAVVVLGDIGRSPRMQYHSMSL SKLENTKVTLIGYRESEPHPQIVNN DSITIEPLKPFPISMSNSFKKIPLI SIFMWPLLAICKVLFQIIQLMYVLL VKVPSPLNTILVQSPPAIPTIFVMQ IVCWIRGVHLVIDWHNLGYTLLKLS LSKSDNHPIIRLAKFIERYFAKNAY AHLFVTNEMKIQLVRDWNLKGKTFV FHDKASPIFKSLTDREQEEFLKTFI NKYSIKGEDKVYIESVISKKSIRNP KQQTSIIISSTSWTQDEDFSILLDA IVKYDIEHAINNNNNKVEEAQDESV VLAENLLFIITGKGPQKEYYQEKIN SLSLKKSRIITVWLDSEDYPKLLAC CDLGVSLHNSSSGIDLPMKVVDMFG CCLPVLAIDFKCIGELVKVNYNGFL FKDSDQLHQLLNQLFTHPTNNNTIT NTNNNKNLILEKMRKNLTKDRETDT WESNWLTIKPLFIPSSSSSSSSSSS SSSSSSSSSSSNSKSKKD |
Purity : | Greater than 90% as determined by SDS-PAGE. |
Applications : | SDS-PAGE |
Notes : | Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week. |
Storage : | Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles. |
Storage Buffer : | Tris/PBS-based buffer, 6% Trehalose, pH 8.0 |
Reconstitution : | We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference. |
Gene Name : | alg1 |
Synonyms : | alg1; mntA; DDB_G0286011; Chitobiosyldiphosphodolichol beta-mannosyltransferase; Asparagine-linked glycosylation protein 1 homolog; Beta-1,4-mannosyltransferase; GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase; GDP-mannose-dolichol diphosphochitobiose man |
UniProt ID : | P90522 |
Gene Name : | alg1 |
Synonyms : | alg1; mntA; DDB_G0286011; Chitobiosyldiphosphodolichol beta-mannosyltransferase; Asparagine-linked glycosylation protein 1 homolog; Beta-1,4-mannosyltransferase; GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase; GDP-mannose-dolichol diphosphochitobiose man |
UniProt ID : | P90522 |
Products Types
◆ Recombinant Protein | ||
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ALG1-2454H | Recombinant Human ALG1 Protein, His (Fc)-Avi-tagged | +Inquiry |
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ALG1-9569H | Recombinant Human ALG1, GST-tagged | +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.
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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。
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