LS-C355402

antibody from LSBio

Targeting: APOA1

Provider product page for LS-C355402

Western blot

ELISA

Immunocytochemistry

Immunohistochemistry

Radioimmunoassay

Antibody data

Antibody Data
Antigen structure
References [0]
Comments [0]
Validations
ELISA [9]
Immunohistochemistry [2]

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Product number: LS-C355402 - Provider product page
Provider: LSBio
Product name: APOA1 / Apolipoprotein A 1 Antibody (clone 513) LS-C355402
Antibody type: Monoclonal
Description: Ion exchange chromatography
Reactivity: Human
Host: Mouse
Isotype: IgG
Antibody clone number: 513
Storage: Short term: store at 4°C. Long term: aliquot and store at -20°C. Avoid freeze-thaw cycles.

APOA1 protein structure - LS-C355402 shown in red.

Supportive validation

Submitted by: LSBio (provider)
Enhanced method: Genetic validation
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit oligoclonal antibody diluted to a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 or recombinant mouse Apo A-1 was added to the plate at concentrations ranging from 1.6-1000ng/ml and incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of an HRP-conjugated rabbit anti-mouse IgG cross-adsorbed secondary antibody was incubated for 30 minutes at room temperature. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Enhanced method: Genetic validation
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit monoclonal antibody at a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 standards ranging from 1.6-1000ng/ml (A) or 100ul of diluted normal human serum or diluted serum from a patient with dyslipidemia (B) were incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of a biotinylated rabbit anti-mouse IgG Superclonal secondary antibody was incubated for 1 hour, followed by Streptavidin-HRP for 30 minutes. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Enhanced method: Genetic validation
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit oligoclonal antibody at a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 standards ranging from 1.6-1000ng/ml (A) or 100ul of diluted normal human serum or diluted serum from a patient with dyslipidemia (B) were incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of a biotinylated rabbit anti-mouse IgG Superclonal secondary antibody was incubated for 1 hour, followed by Streptavidin-HRP for 30 minutes. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit oligoclonal antibody diluted to a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 or recombinant mouse Apo A-1 was added to the plate at concentrations ranging from 1.6-1000ng/ml and incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of an HRP-conjugated rabbit anti-mouse IgG cross-adsorbed secondary antibody was incubated for 30 minutes at room temperature. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit monoclonal antibody at a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 standards ranging from 1.6-1000ng/ml (A) or 100ul of diluted normal human serum or diluted serum from a patient with dyslipidemia (B) were incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of a biotinylated rabbit anti-mouse IgG Superclonal secondary antibody was incubated for 1 hour, followed by Streptavidin-HRP for 30 minutes. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit oligoclonal antibody at a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 standards ranging from 1.6-1000ng/ml (A) or 100ul of diluted normal human serum or diluted serum from a patient with dyslipidemia (B) were incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of a biotinylated rabbit anti-mouse IgG Superclonal secondary antibody was incubated for 1 hour, followed by Streptavidin-HRP for 30 minutes. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit oligoclonal antibody diluted to a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 or recombinant mouse Apo A-1 was added to the plate at concentrations ranging from 1.6-1000ng/ml and incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of an HRP-conjugated rabbit anti-mouse IgG cross-adsorbed secondary antibody was incubated for 30 minutes at room temperature. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit monoclonal antibody at a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 standards ranging from 1.6-1000ng/ml (A) or 100ul of diluted normal human serum or diluted serum from a patient with dyslipidemia (B) were incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of a biotinylated rabbit anti-mouse IgG Superclonal secondary antibody was incubated for 1 hour, followed by Streptavidin-HRP for 30 minutes. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.

Supportive validation

Submitted by: LSBio (provider)
Main image
Experimental details: Sandwich ELISA of Apolipoprotein A-1 was performed by coating wells of a 96-well plate with 100ul of an Apo A-1 rabbit oligoclonal antibody at a concentration of 1 µg/mL in carbonate/bicarbonate buffer overnight at 4C. Wells were blocked with 150ul of StartingBlock T20 (TBS) Blocking Buffer for 30 minutes, and 80ul of recombinant human Apo A-1 standards ranging from 1.6-1000ng/ml (A) or 100ul of diluted normal human serum or diluted serum from a patient with dyslipidemia (B) were incubated for 1 hour at room temperature. The plate was washed with 1X TBST, and 100ul per well of an Apo A-1 mouse monoclonal antibody was added to each well for 1 hour at room temperature. The plate was washed, and 100ul per well of a biotinylated rabbit anti-mouse IgG Superclonal secondary antibody was incubated for 1 hour, followed by Streptavidin-HRP for 30 minutes. Detection was performed using 1-Step Ultra TMB Substrate, followed by Stop Solution. Absorbances were read on a spectrophotometer at 450-550nm.