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Human MOG/Myelin Oligodendrocyte Glycoprotein Protein (MOG-HM101)
$243.00 – $810.00
KACTUS Biosystems Human MOG/Myelin Oligodendrocyte Glycoprotein Protein (MOG-HM101) (catalog No. MOG-HM101) is expressed from HEK293 with His tag at the C-Terminus.It contains Gly30-Gly154.
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Catalog No. | MOG-HM101 |
---|---|
Product Name | Human MOG/Myelin Oligodendrocyte Glycoprotein Protein (MOG-HM101) |
Supplier Name | KACTUS Biosystems |
Brand Name | KACTUS Biosystems |
Synonyms | MOG; MGC26137; MOG Ig-AluB; MOGIG2; BTN6; BTNL11; NRCLP7 |
Species | Human |
Source | HEK293 |
Accession | Q16653 |
Product Tag | C-His |
Biotinylated | no |
Exact Sequence | Gly30-Gly154 |
Molecular Weight | The protein has a predicted MW of 15.4 kDa. Due to glycosylation, the protein migrates to 20-23 kDa based on Tris-Bis PAGE result. |
Form | Lyophilized |
Formulation | Lyophilized from 0.22μm filtered solution in PBS (pH 7.4). Normally 8% trehalose is added as protectant before lyophilization. |
Reconstitution | Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/ml is recommended. Dissolve the lyophilized protein in distilled water. |
Purity | > 95% as determined by Tris-Bis PAGE;> 95% as determined by HPLC |
Endotoxin | Less than 1EU per μg by the LAL method. |
Shipping | Shipped at ambient temperature. |
Stability & Storage | '-20 to -80°C for 12 months as supplied from date of receipt.;-20 to -80°C for 3-6 months in unopened state after reconstitution.;2-8°C for 2-7 days after reconstitution.;Recommend to aliquot the protein into smaller quantities for optimal storage. Please minimize freeze-thaw cycles. |
Note | Products will be shipped from the warehouse in Massachusetts. Promotion is running from time to time. Welcome to send a request for quote to message@sydlabs.com. |
Order Offline | Syd Labs, Inc. 4 Avenue E, Hopkinton, MA 01748 USA. Phone: 1-617-401-8149 Fax: 1-617-606-5019 Email: message@sydlabs.com |
Description
MOG-HM101: Human MOG/Myelin Oligodendrocyte Glycoprotein Protein (MOG-HM101)
Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a rare autoimmune disorder with antibodies against the MOG predominantly involving the optic nerve and spinal cord leading to vision loss and paralysis. When MOG antibody disease involves the brain, the phenotype is similar to acute disseminated encephalomyelitis (ADEM).
Please remember our product information: Human MOG/Myelin Oligodendrocyte Glycoprotein Protein (MOG-HM101) catalog number: MOG-HM101 KACTUS Biosystems
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