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Antikörper

MAD2L1 Antibody

Produktgrößen
50 ug
£186,00
CSB-PA619756LA01HU-50UG
100 ug
£334,00
CSB-PA619756LA01HU-100UG
Über dieses Produkt
SKU:
CSB-PA619756LA01HU
Zusätzliche Namen:
HsMAD2 antibody; MAD 2 antibody; MAD2 like 1 antibody; MAD2 mitotic arrest deficient like 1 antibody; MAD2-like protein 1 antibody; Mad2l1 antibody; MD2L1_HUMAN antibody; Mitotic arrest deficient 2-like protein 1 antibody; Mitotic spindle assembly checkpoint protein MAD2A antibody; REV7 antibody
Anwendung:
ELISA, Immunohistochemistry
Buffer:
Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Klonalität:
Polyclonal
Weitere Details:
Component of the spindle-assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. Required for the execution of the mitotic checkpoint which monitors the process of kinetochore-spindle attachment and inhibits the activity of the anaphase promoting complex by sequestering CDC20 until all chromosomes are aligned at the metaphase plate.
Host:
Rabbit
Immunogen:
Recombinant Human Mitotic spindle assembly checkpoint protein MAD2A protein (2-205AA)
Isotyp:
IgG
Physischer Zustand:
Liquid
Aufreinigung:
Protein G Purified
Reaktivitäten:
Human
Versandbedingungen:
Blue Ice
Lagerbedingungen:
-20[o]C/-70[o]C Avoid freeze/thaw cycles.
Hersteller:
Cusabio
Typ:
Antibody: Polyclonal Antibody
IHC image of CSB-PA619756LA01HU diluted at 1:400 and staining in paraffin-embedded human colon cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
IHC image of CSB-PA619756LA01HU diluted at 1:400 and staining in paraffin-embedded human cervical cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.