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Anti-MOG mAbs

简要描述:

Recognises an epitope which is distinct from M26, M38, M45, M3-8 and M3-31. The epitope recognised is a structural epitope, shown by the lack of recognition of linear MOG peptides. Is unique to recombinant hMOG125 and rMOG125, but is not exposed on recombinant hMOG118; hence this epitope is species-independent, but dependent on the length of the protein (Menge et al, 2011).

产品参数:

Cat. No.:MABL-055

Species:Engineer

Species Reactivity:Rat, Human

Type:Recombinate

Application:Blocking, ELISA, IHC

详细介绍

Key features and details

Cat. No.

MABL-055

Name

Anti-MOG mAbs

Clone No.

AFD-M3-24

From

Recombinant Antibody

Isotype

Engineer antibody

Application

Blocking, ELISA, IHC

Species Reactivity

Rat, Human

Basic Information

Specificity

Recognises an epitope which is   distinct from M26, M38, M45, M3-8 and M3-31. The epitope recognised is a   structural epitope, shown by the lack of recognition of linear MOG peptides.   Is unique to recombinant hMOG125 and rMOG125, but is not exposed on recombinant   hMOG118; hence this epitope is species-independent, but dependent on the   length of the protein (Menge et al, 2011).

Alternative Name

Myelin oligodendrocyte glycoprotein; rMOG

UniProt

Q63349

Immunogen

Callithrix jacchus marmosets were   used, and experimental allergic encephalomyelitis was induced by the   injection of rat MOG (aa1-125) into the marmosettes. The rMOG was expressed   in E. coli and purified to homogeneity. The animals were killed 4-70 days after   the onset of symptoms of EAE. Bone marrow and spleen cells were obtained from   an immunized C. jacchus, the RNA extracted with Trizol reagent and rtPCR used   to generate cloning inserts containing Fab portions of IgGk. Phage display   was then used to select for the MOG-reactive Fab fragments using the pCOMB3H   phage display vector, and binding confirmed using an ELISA.

Application Notes

This antibody has been proposed for   the diagnosis and prognosis of multiple sclerosis (MS) or allergic   encephalomyelitis (EAE) by using competition assays to determine if there are   autoantibodies present in an individual. It has also been proposed that it   could be used to predict the severity of the MS or EAE by detecting the   proportion of conformation-specific autoantibodies to linear epitope   autoantibodies. This antibody has been used in ELISAs and competition assays   to characterise its epitope in relation to other antibodies generated against   MOG. It was originally generated and tested as a Fab fragment (vod Budingen   et al, 2002). Whilst this has been shown to not bind to hMOG, it has been   shown to compete with IgG from MS patients for binding to rMOG (Lalive et al,   2006). Analysis has also been done on the amino acid sequence of this   antibody (von Budingen et al, 2006).

Antibody First Published

von Budingen et al Molecular   characterization of antibody specificities against myelin/oligodendrocyte   glycoprotein in autoimmune demyelination Proc. Natl. Acad. Sci. U.S.A.   99(12), 8207-8212 (2002) PMID:12060766

Note on publication

An analysis of 6 Fab fragments   against epitopes on MOG, identifying at least 4 separate epitopes. Analysis   of these epitopes including competition assays with marmoset auto-antibodies,   human auto-antibodies from MS patients, and confirmation that the epit

COA Information For reference only, actual COA shall prevail

Size

100 μg Purified antibody.

Concentration

1 mg/ml.

Purification

Protein A affinity purified

Buffer

PBS with 0.02% Proclin 300.

Concentration

1 mg/ml.

Storage Recommendation

Store at 4⁰C for up to 3 months. For   longer storage, aliquot and store at - 20⁰C.

 


 


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