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Antikörper

Eri1 Polyclonal Antibody

Produktgrößen
50 ug
£302,00
CAC11281-50UG
100 ug
£454,00
CAC11281-100UG
Über dieses Produkt
SKU:
CAC11281
Zusätzliche Namen:
3' 5' exonuclease ERI 1|3' 5' exonuclease ERI1|3' EXO|3' exoribonuclease|3' HEXO|3' histone mRNA exonuclease 1|3''-5'' exonuclease eri1|3''-5'' exoribonuclease 1|3'EXO|3'HEXO|ERI 1|Eri 1 homolog|Eri-1 homolog|eri1|Eri1 homolog|ERI1_HUMAN|HEXO|Histone mRNA 3' end specific exonuclease|Histone mRNA 3' end specific exoribonuclease|Histone mRNA 3''-end-specific exoribonuclease|Histone mRNA 3''-exonuclease 1|MGC35395|Protein 3''hExo|THEX 1|THEX1|Three prime histone mRNA exonuclease 1
Anwendung:
ELISA, Immunofluorescence, Immunohistochemistry, Western Blot
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Klonalität:
Polyclonal
Weitere Details:
The Eri1 Polyclonal Antibody is applicable for the following applications: ELISA, WB, IHC, IF.
Host:
Rabbit
Immunogen:
ERI1
Isotyp:
IgG
Physischer Zustand:
Liquid
Aufreinigung:
Protein G Purified
Reaktivitäten:
Rat
Versandbedingungen:
Blue Ice
Quelle:
Rabbit
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles., 2-8[o]C Avoid freeze/thaw cycles.
Hersteller:
Biomatik
Typ:
Antibody: Polyclonal Antibody
Catalog Antibody.JPG
Western Blot; Positive WB detected in: Jurkat whole cell lysate; All lanes: ERI1 antibody at 7ug/ml; Secondary; Goat polyclonal to rabbit IgG at 1/50000 dilution; Predicted band size: 41 kDa; Observed band size: 46 kDa
IHC image diluted at 1:400 and staining in paraffin-embedded human testis tissue 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 diluted at 1:400 and staining in paraffin-embedded human small intestine tissue 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.
Immunofluorescence staining of HepG2 cells with CAC11281 at 1:133, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).