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Anti-MOG mAbs

简要描述:

Is displaced by M38 and M45 and is weakly displaced by M26 although this is not mutual which may suggest the M26-mediated displacement is conformationally driven, although this has not been confirmed. The epitope recognised is a structural epitope, shown by the lack of recognition of linear MOG peptides. Binds MOG expressed in CHO cells.

产品参数:

Cat. No.:MABL-056

Species:Engineer

Species Reactivity:Rat, Human

Type:Recombinate

Application:Blocking, ELISA, IHC

详细介绍

Key features and details

Cat. No.

MABL-056

Name

Anti-MOG mAbs

Clone No.

AFD-M3-31

From

Recombinant Antibody

Isotype

Engineer antibody

Application

Blocking, ELISA, IHC

Secies Reactivity

Rat, Human

Basic Information

Specificity

Is displaced by M38 and M45 and is   weakly displaced by M26 although this is not mutual which may suggest the   M26-mediated displacement is conformationally driven, although this has not   been confirmed. The epitope recognised is a structural epitope, shown by the   lack of recognition of linear MOG peptides. Binds MOG expressed in CHO cells.

Alternative Name

Myelin oligodendrocyte glycoprotein; rMOG;   hMOG

UniProt

Q63350

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). This antibody has also shown to bind to hMOG expressed in a CHO   cell line (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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