ARL2BP Polyclonal Antibody, Cat#CAC15833
Western Blot, Positive WB detected in: HepG2 whole cell lysate, U251 whole cell lysate, U87 whole cell lysate, All lanes: ARL2BP antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/50000 dilution, Predicted band size: 19, 18 kDa, Observed band size: 19 kDa
IHC image of CAC15833 diluted at 1:100 and staining in paraffin-embedded human glioma 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.
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ARL2BP Polyclonal Antibody, Cat#CAC15833 Western Blot, Positive WB detected in: HepG2 whole cell lysate, U251 whole cell lysate, U87 whole cell lysate, All lanes: ARL2BP antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/50000 dilution, Predicted band size: 19, 18 kDa, Observed band size: 19 kDa IHC image of CAC15833 diluted at 1:100 and staining in paraffin-embedded human glioma 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.

Ultra Sensitive IHC

ARL2BP Polyclonal Antibody

BiomatikSKU: CAC15833-100ul
Size: 100ul
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Western Blot, Positive WB detected in: HepG2 whole cell lysate, U251 whole cell lysate, U87 whole cell lysate, All lanes: ARL2BP antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/50000 dilution, Predicted band size: 19, 18 kDa, Observed band size: 19 kDa
IHC image of CAC15833 diluted at 1:100 and staining in paraffin-embedded human glioma 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.

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