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Anti-GFAP Antikörper [1B4] (A279081)

$355

Monoklonal [1B4] Maus Antikörper gegen GFAP für WB, IHC-P, IHC-Fr und RIA.

Versandkosten
Vorlaufzeit
Lieferung in 4-6 Werktagen
Telefon
+1 (314) 370-6046
Mo bis Frei, 8am - 4pm AST
Email
orders@antibodies.com

Empfohlene Produkte für Anti-GFAP Antikörper

Produktname
Anti-GFAP Antibody [1B4]
Beschreibung
Mouse monoclonal [1B4] antibody to GFAP.
Spezifität
This antibody recognises glial fibrillary acidic protein, or GFAP, a class III intermediate filament. During development of the central nervous system, GFAP distinguishes astrocytes from other glial cells. It is involved in various cellular functions, such as cell structure and movement, cell communication and the functioning of the blood-brain barrier. It also plays a role in mitosis by adjusting the filament network present in the cell. Defects in GFAP are a cause of Alexander disease, a rare disorder of the central nervous system affecting mostly males. It is a progressive leukoencephalopathy resulting in mental and physical retardation, dementia, seizures and early death. Mouse anti Bovine GFAP antibody, clone 1B4 may be used in conjunction with clones 4A11 and 2E1 for increased sensitivity when used in immunohistology.
Anwendungen
WB, IHC-P, IHC-Fr, RIA
Verdünnungen
IHC-P 1: 1:200 - 1:1,000, WB: 1:200 - 1:2,000
Reaktivität
Bovine, Human, Mouse, Rat, Sheep, Dog, Pig, Rabbit, Guinea Pig, Chicken
Immunogen
Bovine spinal cord homogenate.
Wirt
Mouse
Klonalität
Monoclonal
Klon
1B4
Isotyp
IgG2b
Konjugat

Unconjugated

Reinigung
Protein G affinity chromatography of tissue culture supernatant.
Konzentration
1 mg/ml
Produktform
Liquid
Formulierung
Supplied in Phosphate Buffered Saline with 0.09% Sodium Azide.
Lagerung
Shipped at ambient temperature. Upon delivery aliquot and store at -20°C. When thawed, aliquot the sample as needed. Short term (up to 4 weeks): store at 4°C. Long term: store at -20°C. Avoid freeze / thaw cycles. Storage in frost free freezers is not recommended.
Allgemeine Hinweise
Mouse anti Bovine GFAP antibody, clone 1B4 recognizes glial fibrillary acidic protein, or GFAP, a class III intermediate filament. During development of the central nervous system, GFAP distinguishes astrocytes from other glial cells. It is involved in various cellular functions, such as cell structure and movement, cell communication and the functioning of the blood-brain barrier. It also plays a role in mitosis by adjusting the filament network present in the cell. Defects in GFAP are a cause of Alexander disease, a rare disorder of the central nervous system affecting mostly males. It is a progressive leukoencephalopathy resulting in mental and physical retardation, dementia, seizures and early death. Mouse anti Bovine GFAP antibody, clone 1B4 may be used in conjunction with clones 4A11 and 2E1 for increased sensitivity when used in immunohistology.
Synonyme
ALXDRD, cb345, etID36982.3, FLJ42474, FLJ45472, gfapl, GFAP_HUMAN, Glial fibrillary acidic protein, Intermediate filament protein, wu:fb34h11, wu:fk42c12, xx:af506734, zgc:110485
Haftungsausschluss
Dieses Produkt ist nur für Forschungszwecke bestimmt. Es ist nicht für diagnostische oder therapeutische Zwecke bestimmt.

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