Omentin 298 a.a. Human

Omentin 298 a.a. Human Recombinant
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Description

Biosynthesis and Tissue Distribution

FeatureDetails
Primary expressionVisceral adipose tissue stromal cells (150× higher than subcutaneous)
Secondary sitesOvarian follicles, intestinal Paneth cells, vascular endothelium
Circulatory formDetected in human serum at 200–1,399 ng/ml (age/sex-dependent)

Metabolic Regulation

  • Insulin sensitization: Enhances glucose uptake in adipocytes via Akt phosphorylation, independent of insulin .

  • Lipid metabolism: Correlates inversely with BMI, LDL cholesterol, and triglycerides .

  • Key pathways:

    • AMPK/eNOS activation → Improved endothelial function

    • PPARδ upregulation → Anti-atherogenic effects

Anti-Inflammatory Actions

  • Inhibits TNF-α-induced COX-2 expression via JNK suppression .

  • Reduces NADPH oxidase activity → Decreases vascular oxidative stress .

Clinical Correlations

ConditionOmentin-298 LevelsClinical Impact
Obesity/T2DMMarker of insulin resistance
AtherosclerosisPredicts plaque vulnerability
Polycystic ovary syndromeCorrelates with hyperandrogenism
Rheumatoid arthritisAnti-inflammatory biomarker

Data from ELISA studies showing mean serum concentrations: 486 ng/ml (men), 434 ng/ml (women) .

Recombinant Production and Research Applications

  • Expression system: E.coli-derived, yielding 33.2 kDa non-glycosylated protein .

  • Functional assays:

    • Enhances insulin-stimulated glucose uptake by 47% in adipocytes .

    • Reduces VSMC migration by 62% via HSP27 inhibition .

Detection Methods

  • ELISA specificity: Recognizes epitopes between residues 264–313 with <0.1% cross-reactivity to omentin-2 .

  • Matrix effects: Heparin plasma shows 103% recovery vs serum; avoid EDTA/citrate samples .

Therapeutic Potential

  • Metabolic disorders: Phase I trials exploring omentin supplementation in T2DM .

  • Cardiovascular disease: Preclinical models show 40% reduction in neointimal hyperplasia .

  • Inflammatory bowel disease: Murine studies demonstrate mucosal healing acceleration .

Research Challenges

  • No confirmed cellular receptor identified .

  • Standardization issues: Inter-lab variability in ELISA measurements (CV: 12–18%) .

Product Specs

Introduction
Omentin, primarily found in visceral adipose tissue, is a recently discovered gene highly localized to the mental tissue. Its presence is observed in the stromal vascular cells of adipose tissue, rather than adipocytes. Omentin expression is significantly higher in visceral adipose tissue compared to subcutaneous tissue, with omentin mRNA levels being 150 times greater in the former. Detectable in human blood through western blot analysis, Omentin appears to enhance insulin-stimulated glucose uptake in 3T3-L1 adipocytes in mice. This effect seems to be independent of insulin presence, as Omentin appears to increase Akt phosphorylation regardless. While its role in glucose metabolism and obesity remains to be fully elucidated, an insulin-sensitizing effect is a possibility. Notably, variations in Omentin expression have been observed between adipose tissue from healthy individuals and those with inflammatory bowel disease, although the implications of this difference are yet to be determined.
Description
Recombinant Human Omentin, produced in E. coli, is a single, non-glycosylated polypeptide chain comprising 298 amino acids (17-313). It has a molecular mass of 33.2 kDa and is purified using proprietary chromatographic techniques.
Physical Appearance
A clear, colorless solution that has been sterilized by filtration.
Formulation
Omentin protein is provided at a concentration of 1 mg/ml in a buffer solution containing 20mM Tris-HCL (pH 8), 0.4M Urea, and 10% Glycerol.
Stability
For short-term storage (2-4 weeks), the product can be stored at 4°C. For extended periods, it is recommended to store the product frozen at -20°C. Adding a carrier protein (0.1% HSA or BSA) is advisable for long-term storage. To maintain product integrity, avoid repeated freezing and thawing.
Purity
The purity of the Omentin protein is greater than 90%, as determined by SDS-PAGE analysis.
Synonyms
Intelectin-1, HL1, LFR, HL-1, INTL, ITLN, hIntL.
Source
Escherichia Coli.
Amino Acid Sequence
MWSTDEANTY FKEWTCSSSP SLPRSCKEIK DECPSAFDGL YFLRTENGVI YQTFCDMTSG GGGWTLVASV HENDMRGKCT VGDRWSSQQG SKAVYPEGDG NWANYNTFGS AEAATSDDYK NPGYYDIQAK DLGIWHVPNK SPMQHWRNSS LLRYRTDTGF LQTLGHNLFG IYQKYPVKYG EGKCWTDNGP VIPVVYDFGD AQKTASYYSP YGQREFTAGF VQFRVFNNER AANALCAGMR VTGCNTEHHC IGGGGYFPEA SPQQCGDFSG FDWSGYGTHV GYSSSREITE AAVLLFYR

Q&A

What is the molecular structure of human Omentin/Intelectin-1?

Human Intelectin-1/Omentin is derived from a preproprecursor that is 313 amino acids in length. The protein structure consists of:

  • An 18 amino acid signal sequence

  • A 280 amino acid mature segment (positions 19-298)

  • A 15 amino acid C-terminal segment

The mature protein has a molecular weight of approximately 34 kDa and is encoded by the gene with accession number Q8WWA0 . The protein is primarily produced by visceral adipose tissue, distinguishing it from many other adipokines that are predominantly expressed in subcutaneous adipose tissue .

What are validated detection methods for Omentin in experimental settings?

Multiple validated techniques have demonstrated efficacy in detecting Omentin:

  • Immunohistochemistry/Immunofluorescence: Optimal concentrations range from 0.5-10 μg/mL using affinity-purified polyclonal antibodies. For example, sheep anti-human Intelectin-1/Omentin antibody at 5 μg/mL has shown specific staining in the cytoplasm of U937 human histiocytic lymphoma cells .

  • Tissue-specific localization: Fluorescent immunohistochemistry effectively identifies Omentin in goblet cells of the intestine, where it localizes to mucus granules .

  • Western Blotting: Recommended for protein quantification in tissue lysates.

  • ELISA: Primary method for measuring circulating levels in serum or plasma samples.

Multiple detection methods should be employed for cross-validation of results, particularly when investigating novel tissues or experimental conditions.

What tissue expression patterns have been established for Omentin?

Omentin demonstrates distinct expression patterns across multiple tissues:

  • Primary production site: Visceral adipose tissue

  • Intestinal tissues: Particularly in goblet cells of the ileum, where it localizes to mucus granules

  • Immune cells: Detected in the cytoplasm of U937 human histiocytic lymphoma cell line

  • Evolutionary conservation: Similar expression patterns observed in mouse intestine

This diverse expression profile suggests functions beyond metabolism, potentially including roles in mucosal immunity and intestinal barrier function.

How do Omentin levels correlate with metabolic disorders?

Research consistently demonstrates significant relationships between Omentin levels and metabolic health:

ConditionOmentin Level ChangeAssociated Parameters
ObesityDecreasedIncreased BMI, insulin resistance
Type 1 & 2 DiabetesDecreasedInsulin resistance, hyperglycemia
Polycystic Ovary SyndromeDecreasedInsulin resistance
Cardiovascular DiseaseDecreasedInflammatory markers
Metabolic HealthIncreasedImproved insulin sensitivity

The consistent inverse relationship between Omentin levels and metabolic disorders suggests its potential utility as a biomarker for metabolic health assessment .

What experimental evidence supports Omentin's role in glucose regulation?

Multiple lines of evidence establish Omentin's relationship with glucose homeostasis:

  • Decreased Omentin concentrations are observed in patients with impaired glucose regulation and diabetes (both type 1 and type 2) .

  • Inverse correlations exist between Omentin levels and insulin resistance markers .

  • Experimental Omentin-1 administration in high-fat diet-fed rats significantly decreased glucose, insulin, and HOMA-IR compared to untreated obese controls .

These findings suggest that Omentin likely improves insulin sensitivity through mechanisms that warrant further investigation in molecular signaling studies.

Can dietary interventions modify Omentin expression in research models?

Emerging evidence supports dietary modification of Omentin levels:

  • Athonian-type fasting (AOF): Can significantly increase Omentin levels, which are known to decrease in obesity and type 2 diabetes .

  • Time-restricted eating (TRE): Shows effects on adipokine profiles including Omentin .

  • Energy restriction: Hypocaloric diets (1200-1500 kcal/day for women; 1500-1800 kcal/day for men) combined with time-restricted feeding windows demonstrate improvements in adipokine profiles .

These findings provide methodological guidance for researchers designing interventional studies targeting Omentin modulation.

What animal models are most appropriate for studying Omentin's biological effects?

Rat models have demonstrated particular utility in Omentin research:

  • Diet-induced obesity model: High-fat diet (60% fat, 21% carbohydrate, 18% protein, 5.1 calories/g) for 10 weeks successfully induces obesity and decreases Omentin levels, mimicking human pathophysiology .

  • Intervention protocol: Daily intraperitoneal injections of Omentin-1 (0.2 ml) for 14 consecutive days has shown efficacy in reversing metabolic alterations .

  • Control considerations: Vehicle-treated control groups receiving equivalent volumes of physiologic saline provide appropriate comparisons .

When designing animal experiments, researchers should include comprehensive metabolic assessments including glucose, insulin, lipid parameters, and tissue-specific analyses to fully characterize Omentin's effects.

What methodologies are validated for assessing Omentin's effects on bone metabolism?

The following validated protocols assess bone-related outcomes in Omentin research:

  • Macroscopic assessment: Examination of femur, tibia, and fibula morphology .

  • Quantitative measurements: Dry and ash weight of femur as indicators of bone mineralization .

  • Histological analysis: Longitudinal bone sections assess:

    • Bone thickness

    • Trabecular bone structure

    • Adipocyte content in bone marrow

    • Distribution of hematopoietic tissue

  • Molecular analysis: Gene expression studies of bone metabolism regulators using RT-PCR with primers:

    • mTORC1: forward 5′-ATG ACG AGA CCC AGG CTA AG-3′; reverse 5′-GCC AGT CCT CTA CAA TAC GC-3′

    • AMPK: forward 5′-TGAAGCCAGAGAACGTGTTG-3', reverse 5′-ATAATTTGGCGATCCACAGC-3′

These methodologies provide a comprehensive approach to characterizing Omentin's effects on bone metabolism.

What statistical approaches are recommended for Omentin research?

Based on established methodologies in Omentin studies:

  • Data distribution analysis:

    • Test for normality using D'Agostino–Pearson test

    • Present normally distributed variables as mean ± standard deviation

    • Present non-normally distributed variables as median (interquartile range)

  • Comparative analyses:

    • Student's t-test for normally distributed variables

    • Mann-Whitney test for non-normally distributed variables

  • Longitudinal data:

    • Repeated measures analysis of variance (ANOVA)

    • Logarithmic transformation of non-normally distributed variables before ANOVA

    • Multiple regression analysis to correlate changes in Omentin with simultaneous changes in other parameters

  • Significance thresholds:

    • Standard threshold of p < 0.05 is typically used in Omentin research

What evidence supports Omentin's role in bone metabolism?

Research demonstrates significant effects of Omentin on bone health:

  • High-fat diet-induced obesity leads to significant bone loss in rat models, with decreased dry and ash weight of femur .

  • Omentin-1 treatment antagonizes this bone loss, with significantly higher dry and ash weight of femur in treated versus untreated obese rats .

  • Histological examination reveals that Omentin-1 treatment prevents:

    • Severe thinning of bone

    • Excessive adipocyte infiltration in bone marrow

    • Reduction in trabecular bone formation

These findings suggest potential therapeutic applications for Omentin in preventing obesity-associated bone disorders through mechanisms potentially involving mTORC1 and AMPK signaling pathways.

How does Omentin interact with inflammatory pathways in metabolic research?

While the search results don't provide detailed information on inflammatory pathways, several inferences can be made:

  • Omentin exists within a network of over 600 cytokines (adipokines) produced by adipose tissue that are involved in various metabolic processes including inflammation .

  • Its inverse relationship with obesity and related disorders suggests potential anti-inflammatory properties, as these conditions are characterized by chronic low-grade inflammation .

  • Dietary interventions that increase Omentin (such as Athonian fasting) also reduce vaspin, an adipokine that increases in obesity and type 2 diabetes .

These relationships warrant further investigation into Omentin's potential anti-inflammatory mechanisms through carefully designed molecular signaling studies.

What are promising future research directions for Omentin?

Based on current evidence, several promising research directions emerge:

  • Therapeutic potential in metabolic disorders:

    • Developing recombinant Omentin as a potential therapeutic agent

    • Identifying dietary or pharmacological approaches to enhance endogenous Omentin production

    • Investigating Omentin's effects on insulin signaling pathways

  • Bone metabolism applications:

    • Characterizing molecular mechanisms underlying Omentin's bone-protective effects

    • Assessing potential applications in osteoporosis and other bone disorders

    • Investigating interactions with established bone metabolism regulators

  • Cardiovascular applications:

    • Evaluating Omentin's effects on endothelial function and atherosclerosis

    • Investigating potential cardioprotective mechanisms

  • Methodological advances:

    • Developing standardized assays for Omentin measurement

    • Establishing reference ranges across different populations

    • Creating tissue-specific conditional knockout models

What factors affect reliable measurement of Omentin in research samples?

Several methodological considerations impact Omentin measurement:

  • Preanalytical variables:

    • Fasting status of subjects

    • Time of day for sample collection (potential circadian variation)

    • Sample processing time and temperature

    • Storage conditions and freeze-thaw cycles

  • Analytical variables:

    • Antibody specificity and cross-reactivity

    • Assay sensitivity and dynamic range

    • Calibration standards and quality controls

    • Inter-laboratory variability

  • Biological variables:

    • Age and sex of subjects

    • BMI and body composition

    • Metabolic health status

    • Concurrent medications

Researchers should standardize these variables and include appropriate controls to enhance measurement reliability and cross-study comparisons.

How should researchers address contradictory findings in Omentin research?

When faced with contradictory findings regarding Omentin, researchers should:

  • Evaluate methodological differences:

    • Sample collection methods

    • Assay techniques

    • Sample processing and storage conditions

  • Consider study population heterogeneity:

    • Age and sex distributions

    • Metabolic health status

    • Comorbid conditions

  • Apply appropriate statistical approaches:

    • Meta-analysis of multiple studies

    • Sensitivity analyses to identify sources of heterogeneity

    • Subgroup analyses to identify population-specific effects

  • Examine contextual factors:

    • Dietary patterns of study participants

    • Physical activity levels

    • Medication use that might influence adipokine levels

What ethical considerations apply to Omentin research?

Ethical research practices in Omentin studies include:

  • Human studies:

    • Obtaining appropriate institutional review board approval

    • Securing written informed consent from participants before enrollment

    • Ensuring confidentiality by processing personal information anonymously

  • Animal studies:

    • Following guidelines from the Institute of Laboratory Animal Resources

    • Obtaining approval from institutional animal care and use committees

    • Using appropriate numbers of animals with power calculations

    • Providing proper housing conditions (comfortable temperature, regular light/dark cycles, adequate space)

  • Data reporting:

    • Transparent reporting of methodology

    • Publication of negative results

    • Sharing of raw data when appropriate

These ethical principles ensure research integrity while maximizing scientific value and minimizing harm.

Product Science Overview

Structure and Characteristics

Omentin is a single, non-glycosylated polypeptide chain consisting of 298 amino acids, with a molecular mass of approximately 33.2 kDa . The protein is produced in Escherichia coli (E. coli) and is purified using proprietary chromatographic techniques . The amino acid sequence of Omentin includes regions that are crucial for its biological activity, such as the ability to increase insulin-stimulated glucose uptake .

Expression and Localization

Omentin is predominantly expressed in visceral adipose tissue rather than subcutaneous adipose tissue . It is found in the stromal vascular cells within the adipose tissue, rather than in the adipocytes themselves . This localization is significant because visceral fat is closely associated with metabolic diseases such as diabetes and cardiovascular diseases.

Biological Functions

One of the key functions of Omentin is its role in glucose metabolism. It has been shown to increase insulin-stimulated glucose uptake in adipocytes, which suggests that it may have an insulin-sensitizing effect . Additionally, Omentin has been observed to increase Akt phosphorylation, a process that is crucial for glucose uptake and metabolism .

Production and Stability

The recombinant form of Omentin is produced in E. coli and is supplied as a sterile, filtered colorless solution . The protein is formulated in a buffer containing 20mM Tris-HCL (pH 8), 0.4M Urea, and 10% Glycerol . For optimal stability, it is recommended to store the protein at 4°C if used within 2-4 weeks, or at -20°C for longer periods. Adding a carrier protein, such as 0.1% HSA or BSA, can further enhance its stability .

Research and Applications

Omentin’s role in glucose metabolism and its potential insulin-sensitizing effects make it a promising target for research into metabolic disorders such as diabetes and obesity . Differences in Omentin expression have also been noted in patients with inflammatory bowel disease, although the significance of these findings is still under investigation .

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