Biotin Conjugated Human Lipoprotein A Recombinant Rabbit Monoclonal Antibody [PSH13-82]
cat.: HA723572B
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Cynomolgus monkey
Applications: ELISA(Det), ELISA
Clonality: Monoclonal
Clone number: PSH13-82
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*PBS (pH7.4), 0.1% BSA, 40% Glycerol, 0.05% Proclean 300.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Isotype: IgG
Immunogen: Recombinant protein within Human LPA aa 20-1,033 (HA210979).
Positive control: Recombinant Human Lipoprotein A protein (HA210979).
Subcellular location: Extracellular region, plasma lipoprotein particle.
Recommended Dilutions:
  ELISA(Det)
  ELISA

Use at an assay dependent concentration. Can be paired for Sandwich ELISA with Rabbit monoclonal [PSH13-81] to Human Lipoprotein A antibody (Capture) (HA723570) and recombinant Human Lipoprotein A protein (HA210979) as the standard. The reference range value is 15.6-2,000 pg/mL.
Use at an assay dependent concentration.
Uniprot #: SwissProt: P08519 Human
Alternative names: AK38 Antiangiogenic AK38 protein apo(a) APOA apolipoprotein(a) LP lp(a) LPA
Images
HA723572B_1.jpg Fig1: Sandwich ELISA analysis of human Lipoprotein A matched pair antibodies

Capture: HA723570, Human Lipoprotein A Rabbit mAb [PSH13-81]
Detector: HA723571, Human Lipoprotein A Rabbit mAb [PSH13-82]

Elisa assay was performed by coating wells of a 96-well plate with 50 µl per well of capture antibody (HA723570) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1%BSA blocking buffer, and incubated with serial diluted Recombinant Human Lipoprotein A protein (HA210979) starting from 2,000 pg/ml to 0 pg/ml and detect antibody (HA723571, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 50 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
HA723572B_2.jpg Fig2: Interpolated concentrations of native Lipoprotein A in human urine samples.

Capture: HA723570, Human Lipoprotein A Rabbit mAb [PSH13-81]
Detector: HA723571, Human Lipoprotein A Rabbit mAb [PSH13-82]

The concentrations of Lipoprotein A were measured in duplicates, interpolated from the Lipoprotein A standard curve and corrected for sample dilution. Undiluted samples are human urine 20%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean Lipoprotein A concentration was determined to be 5,193 pg/ml in human urine.
HA723572B_3.jpg Fig3: Interpolated concentrations of native Lipoprotein A in human serum samples.

Capture: HA723570, Human Lipoprotein A Rabbit mAb [PSH13-81]
Detector: HA723571, Human Lipoprotein A Rabbit mAb [PSH13-82]

The concentrations of Lipoprotein A were measured in duplicates, interpolated from the Lipoprotein A standard curve and corrected for sample dilution. Undiluted samples are human serum 0.033%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean Lipoprotein A concentration was determined to be 4.48 µg/ml in human serum.
HA723572B_4.jpg Fig4: Interpolated concentrations of spiked Lipoprotein A in human cell culture media samples.

Capture: HA723570, Human Lipoprotein A Rabbit mAb [PSH13-81]
Detector: HA723571, Human Lipoprotein A Rabbit mAb [PSH13-82]

The concentrations of Lipoprotein A were measured in duplicates, interpolated from the Lipoprotein A standard curves and corrected for sample dilution. Undiluted samples are as follows: cell culture media 50%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.