Anticuerpo policlonal de conejo ACOT4
WB | 1:500 - 1:1000 |
IHC | 1:100 - 1:200 |
FI/CCI | 1:100 - 1:500 |
Descripción | Anticuerpo policlonal de conejo contra ACOT4 |
Especificidad | Reconoce niveles endógenos de proteína ACOT4. |
Tipo de anticuerpo | Anticuerpo primario |
Inmunógeno | KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human ACOT4. The exact sequence is proprietary. |
Purificación | The antibody was purified by immunogen affinity chromatography. |
Peso Molecular | Previsto: 46 kD; Observado: 47 kD |
Formulario/búfer | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
Nombres alternativos | PTE2B; PTEIB; Acyl-coenzyme A thioesterase 4; Acyl-CoA thioesterase 4; PTE-2b; Peroxisomal acyl coenzyme A thioester hydrolase Ib; Peroxisomal long-chain acyl-CoA thioesterase Ib; PTE-Ib |
Símbolo genético | ACOT4 |
Entrez Gene | 122970 (humano); 171282 (ratón) |
SwissProt | Q8N9L9(Humano); Q8BWN8 (ratón) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of ACOT4 expression in U2OS (A), MCF7 (B), mouse lung (C), mouse liver (D), rat lung (E), rat liver (F) whole cell lysates. (Predicted band size: 46 kD; Observed band size: 47 kD)

Immunohistochemical analysis of ACOT4 staining in human liver cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunofluorescent analysis of ACOT4 staining in A549 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
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