GFAP Antikörper

Produktnummer ABIN659067

Dieses Anti-GFAP-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von GFAP in WB, IF und IHC (p). Geeignet für Human. Dieses Primary Antibody wurde in 1 Publikation zitiert.

Kurzübersicht für GFAP Antikörper (ABIN659067)

Target: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser GFAP Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Klon: 183CT3-1-5

Produktdetails anti-GFAP Antikörper

Aufreinigung: This antibody is purified through a protein G column, followed by dialysis against PBS.

Immunogen: This GFAP monoclonal antibody is generated from mouse immunized with GFAP recombinant protein.

Isotyp: IgG2b kappa

Anwendungsinformationen

Applikationshinweise: IF: 1:10~50. WB: 1:4000. WB: 1:100~500. IHC-P-Leica: 1:1000. IHC: 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Haltbarkeit: 6 months

Referenzen für anti-GFAP Antikörper (ABIN659067)

Bajpai, Kerosuo, Tseropoulos, Cummings, Wang, Lei, Liu, Liu, Popescu, Bronner, Andreadis: "Reprogramming Postnatal Human Epidermal Keratinocytes Toward Functional Neural Crest Fates." in: Stem cells (Dayton, Ohio), Vol. 35, Issue 5, pp. 1402-1415, (2018) (PubMed).

Details zu GFAP

Target: GFAP (Glial Fibrillary Acidic Protein (GFAP))

Andere Bezeichnung: GFAP

Hintergrund: This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Molekulargewicht: 49880

Gen-ID: 2670

NCBI Accession: NP_001124491, NP_001229305, NP_002046

UniProt: P14136