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MAB382

Sigma-Aldrich

Anti-Myelin Basic Protein Antibody, a.a. 129-138, clone 1

culture supernatant, clone 1, Chemicon®

Synonym(e):

Myelin A1 protein, Myelin membrane encephalitogenic protein, myelin basic protein

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About This Item

UNSPSC-Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Biologische Quelle

mouse

Qualitätsniveau

Antikörperform

culture supernatant

Antikörper-Produkttyp

primary antibodies

Klon

1, monoclonal

Speziesreaktivität

bovine, rat, rabbit (weakly), human

Darf nicht reagieren mit

guinea pig

Hersteller/Markenname

Chemicon®

Methode(n)

ELISA: suitable
immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
radioimmunoassay: suitable
western blot: suitable

Isotyp

IgG2a

NCBI-Hinterlegungsnummer

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... MBP(4155)
rat ... Mbp(24547)

Allgemeine Beschreibung

The classic group of MBP isoforms (isoforms 4-14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller isoforms might have an important role in remyelination of denuded axons in multiple sclerosis. The non-classic group of MBP isoforms (isoforms 1-3/Golli-MBPs) may preferentially have a role in the early developing brain long before myelination, maybe as components of transcriptional complexes, and may also be involved in signaling pathways in T-cells and neural cells. Differential splicing events combined to optional posttranslational modifications give a wide spectrum of isomers, each of them having maybe a specialized function.

MBP isoforms are found in both the central and the peripheral nervous system, whereas Golli-MBP isoforms are expressed in fetal thymus, spleen and spinal cord, as well as in cell lines derived from the immune system.

Isoform 1 Golli-MBP1, HOG7, 33 kDa

Isoform 2 Golli-MBP2, HOG5, 21.5 kDa

Isoform 3 MBP1, 21.5 kDa

Isoform 4 MBP2, 20.2 kDa

Isoform 5 MBP3, 18.5 kDa

Isoform 6 MBP4, 17.2 kDa

(SP_P02686)

Spezifität

Reacts with MBP from human, bovine and rat, epitope 129-138

Immunogen

Bovine myelin basic protein
Epitope: a.a. 129-138

Anwendung

Research Category
Neurowissenschaft
Research Sub Category
Neuronen- & Gliamarker

Neurochemie & Neurotrophine
Immunohistochemistry(paraffin) Analysis:
Optimal Staining With Citrate Buffer, pH 6.0, Epitope Retrieval: Rat Cerebellum
Immunohistology on frozen sections at 1:10

Western Blot Analysis:
A previous lot of this antibody was used in Western Blot.

ELISA:
A 1:200-1:1,000 dilution of a previous lot was used in ELISA.

RIA:
A previous lot of this antibody was used in Radioimmunoassay.

Optimal working dilutions must be determined by end user.
This Anti-Myelin Basic Protein Antibody, a.a. 129-138, clone 1 is validated for use in ELISA, IH, IH(P), RIA, WB for the detection of Myelin Basic Protein.

Qualität

Routinely evaluated by immunohistochemistry on brain tissue.

Immunohistochemistry(paraffin) Analysis:
MBP (cat. # MAB382) staining pattern/morphology in rat cerebellum. Tissue pretreated with Citrate, pH 6.0. This lot of antibody was diluted to 1:50, using IHC-Select Detection with HRP-DAB. Immunoreactivity is seen as fiber staining in the junction between granular layer and molecular layer.
Optimal Staining With Citrate Buffer, pH 6.0, Epitope Retrieval: Rat Cerebellum

Zielbeschreibung

19 kDa

Physikalische Form

Unpurified
Culture supernatant containing 0.2 M Tris/HCl, pH 7.4 with 5-10% fetal calf serum and 0.1% sodium azide

Lagerung und Haltbarkeit

Stable for 1 year at -20ºC in undiluted aliquots from date of receipt.
Handling Recommendations: Upon receipt, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

Hinweis zur Analyse

Control
Brain tissue

Sonstige Hinweise

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Rechtliche Hinweise

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Haftungsausschluss

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Nucleus-localized 21.5-kDa myelin basic protein promotes oligodendrocyte proliferation and enhances neurite outgrowth in coculture, unlike the plasma membrane-associated 18.5-kDa isoform.
Smith, GS; Samborska, B; Hawley, SP; Klaiman, JM; Gillis, TE; Jones, N; Boggs, JM; Harauz, G
Journal of Neuroscience Research null
Opposing extracellular signal-regulated kinase and Akt pathways control Schwann cell myelination.
Ogata, T; Iijima, S; Hoshikawa, S; Miura, T; Yamamoto, S; Oda, H; Nakamura, K; Tanaka, S
The Journal of Neuroscience null
Induction of oligodendrogenesis in glioblastoma-initiating cells by IFN-mediated activation of STAT3 signaling.
Kanako Yuki, Atsushi Natsume, Hidenori Yokoyama, Yutaka Kondo, Masasuke Ohno et al.
Cancer letters null
Sphingosine kinase 1 and sphingosine 1-phosphate receptor 3 are functionally upregulated on astrocytes under pro-inflammatory conditions.
Fischer, I; Alliod, C; Martinier, N; Newcombe, J; Brana, C; Pouly, S
Testing null
Direct cell-cell interactions control apoptosis and oligodendrocyte marker expression of neuroepithelial cells.
J P Hugnot, K Mellodew, H Pilcher, D Uwanogho, J Price, J D Sinden
Journal of Neuroscience Research null

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