1. Immunology/Inflammation Stem Cell/Wnt MAPK/ERK Pathway Metabolic Enzyme/Protease
  2. Interleukin Related ERK MMP
  3. Anti-IL11RA Antibody (X209)

Anti-IL11RA Antibody (X209)  (Synonyms: EnX209)

Cat. No.: HY-P991219 Purity: 97.75%
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Anti-IL11RA Antibody (X209) (EnX209) is a human-derived IgG4, κ-type antibody inhibitor targeting IL11RA, with a KD of 6 nM. Anti-IL11RA Antibody (X209) blocks the IL11RA signaling pathway, inhibits ERK-dependent activation, and reduces the activation level of ERK1/2. Anti-IL11RA Antibody (X209) exerts a protective effect against fibrosis. Anti-IL11RA Antibody (X209) is applicable to studies related to liver fibrosis, cardiac fibrosis and other related conditions. Recommended isotype control: Human IgG4 kappa, Isotype Control (HY-P99003).

For research use only. We do not sell to patients.

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Description

Anti-IL11RA Antibody (X209) (EnX209) is a human-derived IgG4, κ-type antibody inhibitor targeting IL11RA, with a KD of 6 nM. Anti-IL11RA Antibody (X209) blocks the IL11RA signaling pathway, inhibits ERK-dependent activation, and reduces the activation level of ERK1/2. Anti-IL11RA Antibody (X209) exerts a protective effect against fibrosis. Anti-IL11RA Antibody (X209) is applicable to studies related to liver fibrosis, cardiac fibrosis and other related conditions. Recommended isotype control: Human IgG4 kappa, Isotype Control (HY-P99003)[1][2].

Isotype

Human IgG4 kappa

Recommend Isotype Controls
Species Reactivity

Human

In Vitro

Anti-IL11RA Antibody (X209) (24 h) inhibits the secretion of profibrotic proteins by primary human hepatic stellate cells (HSCs), with an IC50 of 5.4 pM[1].
Anti-IL11RA Antibody (X209) (2 μg/mL; 24 h) inhibits the transformation of primary human hepatic stellate cells (HSCs) into myofibroblasts induced by various NASH-related stimuli[1].
Anti-IL11RA Antibody (X209) (2 μg/mL; 15 min pre-incubation, 48 h co-incubation) potently inhibits Matrigel invasion of primary human hepatic stellate cells (HSCs) induced by PDGF and CCL2[1].
Anti-IL11RA Antibody (X209) (24 h) potently inhibits the secretion of MMP2 and TIMP1 by mouse and human cardiac fibroblasts stimulated with TGFβ1, with an IC50 in the low nM range[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Invasion Assay[1]

Cell Line: Primary human hepatic stellate cells (HSCs)
Concentration: 2 μg/mL
Incubation Time: 15 min (pre-incubation); 48 h (co-incubation with stimulus)
Result: Reduced PDGF/CCL2-induced HSC invasion compared to IgG-treated controls.
In Vivo

Anti-IL11RA Antibody (X209) (10 mg/kg; s.c.; bi-weekly; 4 weeks) abolishes ERK activation, alleviates liver fibrosis and hepatocellular injury, and regulates the expression of profibrotic genes in mice with established NASH[1].
Anti-IL11RA Antibody (X209) (10 mg/kg; i.p.; three times weekly; 7 weeks) reduces liver fibrosis levels and inflammatory gene expression in mice with advanced non-alcoholic steatohepatitis (NASH) induced by Streptozotocin (HY-13753)[1].
Anti-IL11RA Antibody (X209) (20 mg/kg; i.p.; bi-weekly; 2 weeks) significantly attenuates AAC-induced cardiac fibrosis and ERK1/2 activation in male C57BL/6J mice[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6NTac (male, 5 weeks old, fed high fat methionine- and choline-deficient diet for 6 weeks to induce NASH)[1]
Dosage: 10 mg/kg
Administration: s.c.; bi-weekly; 4 weeks
Result: Abolished hepatic ERK activation.
Reduced relative liver hydroxyproline.
Reduced serum ALT levels.
Did not alter hepatic steatosis.
Reduced mRNA expression of pro-fibrotic genes (Col1a1, Col1a2, Col3a1, Acta2, Timp1) and TGFβ1.
Increased Mmp2 mRNA expression.
Animal Model: C57BL/6J (male, 10-12 weeks old; cardiac fibrosis induced via ascending aortic constriction surgery)[2]
Dosage: 20 mg/kg
Administration: i.p.; bi-weekly; 2 weeks
Result: Partially reduced AAC-induced cardiac IL11 protein expression.
Reduced AAC-induced extracellular matrix gene RNA expression, including Col1a1, Col1a2, Col3a1, Fn1, Mmp2, and Timp1.
Significantly reduced AAC-induced myocardial collagen I and III protein expression .
Significantly reduced total myocardial collagen and perivascular fibrosis.
Significantly reduced AAC-induced cardiac ERK1/2 phosphorylation.
Reduced indexed aortic root diameter, and showed significantly higher peak aortic velocity and pressure gradient.
Did not affect post-operative mortality, body weight recovery, terminal body weight, or AAC-induced cardiac hypertrophy.
Application

ELISA, FACS, Functional assay

Conjugated

Unconjugated

Reconsititution

The product can be reconstituted/diluted with sterile PBS or saline.

Molecular Weight

145 kDa

Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Anti-IL11RA Antibody (X209)]

Shipping

Shipping with dry ice.

Formulation

Please refer to the lot-specific COA for specific buffer information.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Biological Activity
  • Flow Cytometry analysis of K562 cells labelling IL-11RA (red) with Anti-IL11RA Antibody (HY-P991219). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then cells were stained with the primary antibody at 1/200 dilution for an hour at 4℃. Goat Anti-Human IgG H&L (AF488) (HY-P83776) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Human IgG4 kappa (HY-P99003, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).
Purity & Documentation
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Anti-IL11RA Antibody (X209)
Cat. No.:
HY-P991219
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