ADRB1 ELISA Kit

Catalog No. ABIN5651472

Product Details ADRB1 ELISA Kit

Target: ADRB1 (Adrenergic, beta-1-, Receptor (ADRB1))

Reactivity: Human

Detection Method: Colorimetric

Method Type: Sandwich ELISA

Detection Range: 0.312 ng/mL - 20 ng/mL

Minimum Detection Limit: 0.312 ng/mL

Application: ELISA

Sample Type: Cell Lysate, Tissue Homogenate

Analytical Method: Quantitative

Specificity: This assay has high sensitivity and excellent specificity for detection of Adrenergic Receptor Beta 1 (ADRb1). No significant cross-reactivity or interference between Adrenergic Receptor Beta 1 (ADRb1) and analogues was observed.

Sensitivity: 0.122 ng/mL

Application Details

Comment:

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Assay Time: 3 h

Plate: Pre-coated

Protocol: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Adrenergic Receptor Beta 1 (ADRb1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Adrenergic Receptor Beta 1 (ADRb1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Adrenergic Receptor Beta 1 (ADRb1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Adrenergic Receptor Beta 1 (ADRb1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Assay Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Adrenergic Receptor Beta 1 (ADRb1) were tested 20 times on one plate, respectively
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Adrenergic Receptor Beta 1 (ADRb1) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Restrictions: For Research Use only

Handling

Handling Advice: The Stop Solution is acidic. Do not allow to contact skin or eyes. Calibrators, controls and specimen samples should be assayed in duplicate. Once the procedure has been started, all steps should be completed without interruption.

Storage: 4 °C,-20 °C

Storage Comment: -20°C. Bring all reagents to room temperature before beginning test. The kit may be stored at 4°C for immediate use within two days upon arrival. Reseal any unused strips with desiccant pack. Minimize freeze/thaw cycles.

Expiry Date: 4-8 months

Target Details for ADRB1

Target: ADRB1 (Adrenergic, beta-1-, Receptor (ADRB1))

Alternative Name: Adrenergic Receptor Beta 1 (ADRB1 Products)

Synonyms: ADRB1R ELISA Kit, B1AR ELISA Kit, BETA1AR ELISA Kit, RHR ELISA Kit, RATB1AR ELISA Kit, X-Beta1AR ELISA Kit, BAR1 ELISA Kit, zgc:194728 ELISA Kit, zgc:194731 ELISA Kit, ADRB1 ELISA Kit, Adrb-1 ELISA Kit, beta-AR ELISA Kit, adrenoceptor beta 1 ELISA Kit, adrenoceptor beta 1 L homeolog ELISA Kit, adrenergic, beta-1-, receptor ELISA Kit, adrenergic receptor, beta 1 ELISA Kit, ADRB1 ELISA Kit, Adrb1 ELISA Kit, adrb1.L ELISA Kit, adrb1 ELISA Kit

Background:

Gene Name: Adrenergic Receptor Beta 1

Gene Aliases: ADR-B1, ADRB1R, B1AR, BETA1AR, RHR, Beta 1 Adrenoreceptor, Beta-1 adrenoceptor

Pathways: cAMP Metabolic Process, Cellular Glucan Metabolic Process, Regulation of Muscle Cell Differentiation, Synaptic Membrane, Regulation of G-Protein Coupled Receptor Protein Signaling, G-protein mediated Events, Interaction of EGFR with phospholipase C-gamma, Brown Fat Cell Differentiation