Mammalian INHBE enzyme-linked immunoassay kit (one step)

CAT: EHY0245 Datasheet
Specification 96 Test
Sensitivity 0.06 ng/ml (10 μl)
Standard Curve Range 3.91~250 ng/ml
Standard Curve Gradient 7 Points
Number of Incubations 2
Detectable sample serum, plasma
Sample Volume 10 μl
Type Fully Ready-to-Use
Operation Duration 60 min
ng/ml O.D. Average Corrected
0.00 0.0073 0.0065 0.0069
3.91 0.0656 0.0629 0.0643 0.0574
7.81 0.1209 0.1289 0.1249 0.1180
15.63 0.2501 0.2472 0.2487 0.2418
31.25 0.5334 0.4981 0.5158 0.5089
62.50 1.0980 1.0110 1.0545 1.0476
125.00 2.0750 1.8970 1.9860 1.9791
250.00 3.2990 3.0870 3.1930 3.1861

Precision

Intra-assay Precision Inter-assay Precision
Sample Number S1 S2 S3 S1 S2 S3
22 22 22 6 6 6
Average(ng/ml) 3.4 15.1 45.8 4.2 20.0 53.8
Standard Deviation 0.1 0.6 2.3 0.2 0.6 1.3
Coefficient of Variation(%) 2.6 3.7 4.9 4.7 3.2 2.4

Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays) Three samples of known concentration were tested six times on one plate to assess intra-assay precision.

Spike Recovery

The spike recovery was evaluated by spiking 3 levels of Mammalian INHBE into health mammal serum sample. The un-spiked serum was used as blank in this experiment.
The recovery ranged from 80% to 119% with an overall mean recovery of 96%.

Sample Values

Sample Matrix Sample Evaluated Range (ng/ml) Detectable (%) Mean of Detectable (ng/ml)
Human Serum303.22-282.5410030.90
Mouse Serum306.54-28.0810013.48
Rat Serum303.39-149.3310031.78
Monkey Serum29.74-10.171009.95

Serum/Plasma – samples from apparently healthy mammals were evaluated for the presence of INHBE in this assay.

Background: INHBE

Inhibin beta E (INHBE) is a member of the transforming growth factor-beta (TGF-beta ) superfamily of cytokines, with a molecular weight of approximately 40 kDa. INHBE plays critical roles in the regulation of diverse physiological processes, including cell growth, differentiation, and metabolism. It is a key component of the activin signaling pathway, where it dimerizes with other beta -subunits to form bioactive ligands involved in endocrine regulation. INHBE is primarily expressed in hepatic and reproductive tissues and has been implicated in metabolic homeostasis, particularly in energy expenditure and glucose metabolism. Dysregulation of INHBE expression has been linked to pathophysiological conditions such as obesity, insulin resistance, and liver disease. Furthermore, INHBE has gained attention for its tumor-suppressive role in certain cancers, suggesting its potential as a regulator of cell proliferation and apoptosis. Its specificity and involvement in metabolic and oncogenic pathways highlight INHBE as a promising biomarker and a potential target for therapeutic strategies.

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