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Picoamh elisa kit

Manufactured by Ansh Labs
Sourced in United States

The PicoAMH ELISA kit is a laboratory diagnostic tool designed to measure Anti-Müllerian Hormone (AMH) levels in biological samples. AMH is a protein produced by the granulosa cells of the ovarian follicles, and its measurement provides information about ovarian reserve and function. The PicoAMH ELISA kit utilizes an enzyme-linked immunosorbent assay (ELISA) technique to quantify AMH concentrations in the tested samples.

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5 protocols using picoamh elisa kit

1

Relative Telomere Length and AMH Quantification

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Whole blood relative LTL was measured by multiplex quantitative polymerase chain reaction (MMqPCR) as previously described [38 ,39 (link)]. AMH levels were quantified using the picoAMH ELISA kit (product ID: AL-124, Ansh Labs, Webster, Texas, USA) as per manufacturer instructions. The linear range of this assay is between 25–6000 pg/ml. AMH measurements that fell below the limit of detection are reported as at the limit of detection. More information is found in the supplement.
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2

Ultrasensitive AMH ELISA Protocols

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Assays of AMH concentrations in serum samples were performed at the Reproductive Endocrine Research Laboratory at the University of Southern California Keck School of Medicine. An Ultrasensitive AMH ELISA kit (Ansh Labs, Webster TX) was used to measure AMH. The interassay coefficients of variation for the Ultrasensitive AMH ELISA are 4.6%, 4.8%, and 2.0% at 0.346, 0.715, and 1.85 ng/ml, respectively. When AMH values were below the limit of detection of this instrument (<0.07 ng/ml), the picoAMH ELISA kit (Ansh Labs), was used. The picoAMH ELISA has a limit of detection of 0.003 ng/ml, and interassay coefficients of 4.5%, 2.2%, and 3.8% at 22.6, 86.5, and 373 pg/ml, respectively. A total of 12 samples had undetectable concentrations using the picoAMH.
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3

Serum AMH Quantification Protocol

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Blood samples were collected at the DISC06 follow-up visit in the morning after an overnight fast by venipuncture using standard procedures. Blood was allowed to stand at room temperature for 45 minutes to allow complete clotting. Blood was then centrifuged and serum was separated and pipetted in 0.5 mL aliquots into cryovials, which were labeled and stored at −80°C.
AMH was measured in serum using single lot of picoAMH ELISA kit (AL-124, Ansh Labs, Webster, TX) (38 ). The limit of detection (LOD) of the picoAMH ELISA is 1.2 pg/mL; no participant samples were below the LOD. The manufacturer-specified interassay coefficients of variation (CVs) are 4.5%, 2.2%, and 3.8% at 22.6, 86.5, and 373 pg/mL, respectively, for the picoAMH assays. Internal quality control samples included in the assay run resulted in CVs of 3.2% and 4.0% at mean AMH concentrations of 91.2 and 285 pg/mL, respectively. Finally, four participant samples were run in duplicate with mean CV of 4.7%.
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4

Measuring AMH Levels with Ultrasensitive ELISA

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AMH assays were performed at the Reproductive Endocrine Research Laboratory at the University of Southern California Keck School of Medicine. AMH was measured primarily using an Ultrasensitive AMH ELISA kit (Ansh Labs, Webster, TX). However, when AMH levels were below the limit of detection of the Ultrasensitive ELISA (<0.07 ng/ml), the picoAMH ELISA kit (Ansh Labs) was used and recovered levels for 83 control samples. The limit of detection of the picoAMH ELISA is 0.003 ng/ml.
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5

Ultrasensitive AMH Assay Protocol

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All assays were performed at the Reproductive Endocrinology laboratory at the University of Southern California Keck School of Medicine. Case-control trios were analyzed together in the same batch. AMH was measured primarily using an Ultrasensitive AMH ELISA kit (Ansh Labs, Webster, TX). The picoAMH ELISA kit (Ansh Labs) was used when AMH values were below the limit of detection of the Ultrasensitive ELISA (<0.07 ng/ml). The limit of detection of the picoAMH ELISA is 0.003 ng/ml. Of the 1,354 samples, 484 (154 cases, 330 controls) did not have detectable levels by the Ultrasensitive ELISA and were analyzed by the picoAMH ELISA. Of these, 130 (47 cases, 83 controls) had detectable concentrations using the picoAMH. The manufacturer-specified interassay coefficients of variation are as follows: 4.6%, 4.8% and 2.0% at 0.346, 0.715 and 1.85 ng/ml, respectively, for the Ultrasensitive AMH assay, and 4.5%, 2.2% and 3.8% at 22.6, 86.5 and 373 pg/ml, for the picoAMH assays. In our study, blinded control samples (mean=1.89 ng/ml) were run in duplicate in the first 39 batches with interassay CVs of 14.5%. Testosterone was measured by radioimmunoassay with preceding organic solvent extraction and Celite column partition chromatography (16 (link)). The assay sensitivity is 1.5 ng/dL and the interassay CVs are 8%, 12% and 12% at 13, 30 and 96 ng/dL, respectively.
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