ARG80779
Human Intact PTH / Parathyroid Hormone ELISA Kit
Human Intact PTH / Parathyroid Hormone ELISA Kit for ELISA and Human
Signaling Transduction kit
Overview
Product Description | ARG80779 Human Intact PTH / Parathyroid Hormone ELISA Kit is intended for the quantification of Intact-PTH (Parathyroid Hormone) in human serum and plasma (EDTA). |
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Tested Reactivity | Hu |
Tested Application | ELISA |
Target Name | Intact PTH / Parathyroid Hormone |
Conjugation | HRP |
Conjugation Note | Substrate: TMB and read at 450 nm or 405 nm |
Sensitivity | 1.57 pg/ml |
Sample Type | Serum and plasma (EDTA). |
Standard Range | 11.1 - 971 pg/ml |
Sample Volume | 25 µl |
Alternate Names | PTH1; Parathyroid hormone; Parathyrin; Parathormone; PTH |
Application Instructions
Assay Time | 3 h, 30 min (RT/shaker) |
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Properties
Form | 96 well |
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Storage Instruction | Store the kit at 2-8°C. Keep microplate wells sealed in a dry bag with desiccants. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Gene Symbol | PTH |
Gene Full Name | parathyroid hormone |
Background | PTH (Parathyroid hormone, Parathormone, Parathyrin) is biosynthesized in the parathyroid gland as a pre-proparathyroid hormone, a larger molecular precursor consisting of 115 amino acids. Following sequential intracellular cleavage of a 25-amino acid sequence, preproparathyroid hormone is converted to an intermediate, a 90-amino acid polypetide, proparathyroid hormone. With additional proteolytic modification, proparathyroid hormone is then converted to parathyroid hormone, an 84 amino acid polypeptide. In healthy individuals, regulation of parathyroid hormone secretion normally occurs via a negative feedback action of serum calcium on the parathyroid glands. Intact PTH is biologically active and clears very rapidly from the circulation with a half-life of less than four minutes. PTH undergoes proteolysis in the parathyroid glands, but mostly peripherally, particularly in the liver but also in the kidneys and bone, to give N-terminal fragments and longer lived C-terminal and midregion fragments. In subjects with renal insufficiency, C‑terminal and midregion PTH assays typically give elevated PTH results, as reflected by impaired renal clearance. Intact PTH assays are important for the differentiation of primary hyperparathyroidism from other (non-parathyroid-mediated) forms of hypercalcemia, such as malignancy, sarcoidosis and thyrotoxicosis. The measurement of parathyroid hormone is the most specific way of making the diagnosis of primary hyperparathyroidism. In the presence of hypercalcemia, an elevated level of parathyroid hormone virtually establishes the diagnosis. In over 90% of patients with primary hyperparathyroidism, the parathyroid hormone will be elevated. The most common other cause of hypercalcemia, namely hypercalcemia of malignancy, is associated with suppressed levels of parathyroid hormone or PTH levels within the normal range. When intact PTH level is plotted against serum calcium, the intact PTH concentration for patients with hypercalcemia of malignancy is almost always found to be inappropriately low when interpreted in view of the elevated serum calcium. Unlike C-terminal and midregion PTH, which typically are grossly elevated in subjects with renal insufficiency, intact PTH assays are less influenced by the declining renal function. PTH values are typically undetectable in hypocalcemia due to total hypoparathyroidism, but are found within the normal range in hypocalcemia due to partial loss or inhibition of parathyroid function. |
Highlight | Related products: PTH antibodies; PTH ELISA Kits; PTH Duos / Panels; New ELISA data calculation tool: Simplify the ELISA analysis by GainData |
Research Area | Signaling Transduction kit |
Title | Download Link |
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ARG80779 Human Intact PTH / Parathyroid Hormone ELISA Kit User's manual | Download |