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Antibodies

Fasn Polyclonal Antibody

Product Sizes
50 ug
£302.00
CAC07284-50UG
100 ug
£454.00
CAC07284-100UG
About this Product
SKU:
CAC07284
Additional Names:
[Acyl-carrier-protein] S acetyltransferase|[Acyl-carrier-protein] S malonyltransferase|3-hydroxypalmitoyl-[acyl-carrier-protein] dehydratase|3-oxoacyl-[acyl-carrier-protein] reductase|3-oxoacyl-[acyl-carrier-protein] synthase|Enoyl-[acyl-carrier-protein] reductase|FAS|FAS_HUMAN|FASN|Fatty acid synthase|MGC14367|MGC15706|OA 519|Oleoyl-[acyl-carrier-protein] hydrolase|SDR27X1|Short chain dehydrogenase/reductase family 27X member 1
Application:
ELISA, Immunofluorescence, Immunohistochemistry
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Clonality:
Polyclonal
Extra Details:
The Fasn Polyclonal Antibody is applicable for the following applications: ELISA, IHC, IF.
Host:
Rabbit
Immunogen:
FASN
Isotype:
IgG
Physical State:
Liquid
Purification:
Protein G Purified
Shipping Conditions:
Blue Ice
Source:
Rabbit
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles., 2-8[o]C Avoid freeze/thaw cycles.
Supplier:
Biomatik
Type:
Antibody: Polyclonal Antibody
Catalog Antibody.JPG
IHC image of CAC07284 diluted at 1:100 and staining in paraffin-embedded human breast 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 diluted at 1:100 and staining in paraffin-embedded human liver 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 ABC system.
Immunofluorescence staining of Hela cells with CAC07284 at 1:100, 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).