Mammalian Activin E 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-two 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 Activin E 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 Activin E in this assay.

Background: Activin E

Activin E, encoded by the INHBE gene, is a liver-enriched member of the transforming growth factor-beta (TGF-beta ) superfamily and functions as a hepatokine involved in systemic energy homeostasis. Structurally, it is a disulfide-linked homodimer of mature inhibin beta E subunits, sharing the conserved cystine-knot motif characteristic of TGF-beta ligands, which facilitates receptor binding and downstream signaling activation. Activin E signals through the type I receptor ALK7 (ACVR1C), activating the SMAD2/3 pathway and repressing PPARG target genes in adipose tissue. This signaling cascade suppresses beta -adrenergic-induced lipolysis, thereby promoting lipid retention in white adipose tissue and preventing excessive hepatic lipid influx during metabolic stress such as fasting. In murine models, mRNA knocked down results in increased fat oxidation, reduced adiposity, and improved metabolic profiles under high-fat diet conditions. Conversely, hepatic overexpression of INHBE leads to visceral fat accumulation and adipocyte hypertrophy, indicating a maladaptive role in obesity . Rare loss-of-function variants in human INHBE are associated with favorable fat distribution and reduced risk of type 2 diabetes, highlighting its clinical relevance. Expression of INHBE is upregulated by ATF4 during endoplasmic reticulum stress, linking it to nutrient sensing and adaptive metabolic responses. These findings underscore the potential of recombinant Activin E as a therapeutic target for metabolic disorders such as nonalcoholic fatty liver disease (NAFLD) and obesity.

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