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Antibodies

Gpt Polyclonal Antibody

Product Sizes
50 ug
£302.00
CAC08496-50UG
100 ug
£454.00
CAC08496-100UG
About this Product
SKU:
CAC08496
Additional Names:
AAT1|Alanine aminotransferase|Alanine aminotransferase 1|ALAT1_HUMAN|ALT1|Glutamate pyruvate transaminase 1|Glutamic alanine transaminase 1|Glutamic pyruvate transaminase (alanine aminotransferase)|Glutamic pyruvic transaminase 1|Glutamic--alanine transaminase 1|Glutamic--pyruvic transaminase 1|gpt|GPT 1|GPT1
Application:
ELISA, Immunofluorescence, Immunohistochemistry, Immunoprecipitation, Western Blot
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Clonality:
Polyclonal
Extra Details:
The Gpt Polyclonal Antibody is applicable for the following applications: ELISA, WB, IHC, IF, IP.
Host:
Rabbit
Immunogen:
GPT
Isotype:
IgG
Physical State:
Liquid
Purification:
Protein G Purified
Reactivities:
Mouse, Rat
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 CAC08496 diluted at 1:350 and staining in paraffin-embedded human kidney 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.
Immunofluorescent analysis of HepG2 cells using CAC08496 at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
Western Blot; , Positive WB detected in: HepG2 whole cell lysate, Rat liver tissue, Mouse liver tissue; , All lanes: GPT antibody at 4.5ug/ml; , Secondary; , Goat polyclonal to rabbit IgG at 1/50000 dilution; , Predicted band size: 55 kDa; , Observed band size: 55 kDa
IHC image diluted at 1:350 and staining in paraffin-embedded human liver 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.