Mouse IL-27A p28 Recombinant Rabbit Monoclonal Antibody [PSH14-32] - BSA and Azide free (Detector)
Overview
Product Name
Mouse IL-27A p28 Recombinant Rabbit Monoclonal Antibody [PSH14-32] - BSA and Azide free (Detector)
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Recombinant protein within Mouse IL-27A p28 aa 29-234 (HA211005).
Species Reactivity
Mouse
Validated Applications
ELISA(Det)
Positive Control
Recombinant Mouse IL-27A p28 protein (HA211005).
Conjugation
unconjugated
Clone Number
PSH14-32
Product Features
Form
Liquid
Concentration
1mg/ml
Storage Instructions
Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage Buffer
1*PBS (pH7.4).
Isotype
IgG
Purification Method
Protein A affinity purified.
Application Dilution
-
ELISA(Det)
-
Use at an assay dependent concentration. Can be paired for Sandwich ELISA with Rabbit monoclonal [PSH14-31] to Mouse IL-27A p28 antibody (Capture) (HA723624) or Rabbit monoclonal [PSH14-33] to Mouse IL-27A p28 antibody (Capture) (HA723627) and Recombinant Mouse IL-27A p28 protein (HA211005) as the standard. The reference range value is 7.8-1,000 pg/mL.
Target
Function
Associates with EBI3 to form the IL-27 interleukin, a heterodimeric cytokine which functions in innate immunity. IL-27 has pro- and anti-inflammatory properties, that can regulate T-helper cell development, suppress T-cell proliferation, stimulate cytotoxic T-cell activity, induce isotype switching in B-cells, and that has diverse effects on innate immune cells. Among its target cells are CD4 T-helper cells which can differentiate in type 1 effector cells (TH1), type 2 effector cells (TH2) and IL17 producing helper T-cells (TH17). It drives rapid clonal expansion of naive but not memory CD4 T-cells. It also strongly synergizes with IL-12 to trigger interferon-gamma/IFN-gamma production of naive CD4 T-cells, binds to the cytokine receptor WSX-1/TCCR which appears to be required but not sufficient for IL-27-mediated signal transduction. IL-27 potentiate the early phase of TH1 response and suppress TH2 and TH17 differentiation. It induces the differentiation of TH1 cells via two distinct pathways, p38 MAPK/TBX21- and ICAM1/ITGAL/ERK-dependent pathways. It also induces STAT1, STAT3, STAT4 and STAT5 phosphorylation and activates TBX21/T-Bet via STAT1 with resulting IL12RB2 up-regulation, an event crucial to TH1 cell commitment. It suppresses the expression of GATA3, the inhibitor TH1 cells development. In CD8 T-cells, it activates STATs as well as GZMB. IL-27 reveals to be a potent inhibitor of TH17 cell development and of IL-17 production. Indeed IL27 alone is also able to inhibit the production of IL17 by CD4 and CD8 T-cells. While IL-27 suppressed the development of pro-inflammatory Th17 cells via STAT1, it inhibits the development of anti-inflammatory inducible regulatory T-cells, iTreg, independently of STAT1. IL-27 also has an effect on cytokine production, it suppresses pro-inflammatory cytokine production such as IL2, IL4, IL5 and IL6 and activates suppressors of cytokine signaling such as SOCS1 and SOCS3.
Background References
1. Feng X.M., Chen X.L., Liu N., Chen Z., Zhou Y.L., Han Z.B., Zhang L., Han Z.C. Interleukin-27 upregulates major histocompatibility complex class II expression in primary human endothelial cells through induction of major histocompatibility complex class II transactivator. Hum. Immunol. 68:965-972 (2007)
2. Fakruddin J.M., Lempicki R.A., Gorelick R.J., Yang J., Adelsberger J.W., Garcia-Pineres A.J., Pinto L.A., Lane H.C., Imamichi T. Noninfectious papilloma virus-like particles inhibit HIV-1 replication: implications for immune control of HIV-1 infection by IL-27. Blood 109:1841-1849 (2007)
Subcellular Location
Secreted.
UNIPROT
Synonyms
EBI3 antibody
IL 27 antibody
IL 27 p28 subunit antibody
IL 27A antibody
IL 30 antibody
IL-27 subunit alpha antibody
IL-27-A antibody
IL27 antibody
IL27-A antibody
IL27A antibody
ExpandImages
-
![Sandwich ELISA analysis of Mouse IL-27A p28 matched pair antibodies<br /><br />Capture: <a href="/products/HA723624" style="font-weight: bold;text-decoration: underline;">HA723624</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-31]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (<a href="/products/HA723624" style="font-weight: bold;text-decoration: underline;">HA723624</a>) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Mouse IL-27A p28 protein (<a href="/products/HA211005" style="font-weight: bold;text-decoration: underline;">HA211005</a>) starting from 1,000 pg/ml to 0 pg/ml and detect antibody (<a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.](https://storage.huabio.cn/huabio/productImg/HA723625_1.png?v=20260429162005)
Sandwich ELISA analysis of Mouse IL-27A p28 matched pair antibodies
Capture: HA723624, Mouse IL-27A p28 Rabbit mAb [PSH14-31]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA723624) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Mouse IL-27A p28 protein (HA211005) starting from 1,000 pg/ml to 0 pg/ml and detect antibody (HA723625, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm. -
![Sandwich ELISA analysis of Mouse IL-27A p28 matched pair antibodies<br /><br />Capture: <a href="/products/HA723627" style="font-weight: bold;text-decoration: underline;">HA723627</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-33]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (<a href="/products/HA723627" style="font-weight: bold;text-decoration: underline;">HA723627</a>) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Mouse IL-27A p28 protein (<a href="/products/HA211005" style="font-weight: bold;text-decoration: underline;">HA211005</a>) starting from 1,000 pg/ml to 0 pg/ml and detect antibody (<a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.](https://storage.huabio.cn/huabio/productImg/HA723625_2.png?v=20260429162005)
Sandwich ELISA analysis of Mouse IL-27A p28 matched pair antibodies
Capture: HA723627, Mouse IL-27A p28 Rabbit mAb [PSH14-33]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA723627) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Mouse IL-27A p28 protein (HA211005) starting from 1,000 pg/ml to 0 pg/ml and detect antibody (HA723625, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm. -
![Interpolated concentrations of native IL-27A p28 in LPS stimulated RAW 264.7 cell culture supernatant.<br /><br />Capture: <a href="/products/HA723624" style="font-weight: bold;text-decoration: underline;">HA723624</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-31]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />RAW 264.7 cells were cultured for 48 hours and stimulated with 5 µg/ml LPS. The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are stimulated RAW 264.7 cell culture supernatant 100%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean IL-27A p28 concentration was to be 2,074 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant.](https://storage.huabio.cn/huabio/productImg/HA723625_3.png?v=20260429162005)
Interpolated concentrations of native IL-27A p28 in LPS stimulated RAW 264.7 cell culture supernatant.
Capture: HA723624, Mouse IL-27A p28 Rabbit mAb [PSH14-31]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
RAW 264.7 cells were cultured for 48 hours and stimulated with 5 µg/ml LPS. The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are stimulated RAW 264.7 cell culture supernatant 100%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean IL-27A p28 concentration was to be 2,074 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant. -
![Interpolated concentrations of native IL-27A p28 in LPS stimulated RAW 264.7 cell culture supernatant.<br /><br />Capture: <a href="/products/HA723627" style="font-weight: bold;text-decoration: underline;">HA723627</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-33]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />RAW 264.7 cells were cultured for 48 hours and stimulated with 5 µg/ml LPS. The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are stimulated RAW 264.7 cell culture supernatant 100%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean IL-27A p28 concentration was to be 1,264 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant.](https://storage.huabio.cn/huabio/productImg/HA723625_4.png?v=20260429162005)
Interpolated concentrations of native IL-27A p28 in LPS stimulated RAW 264.7 cell culture supernatant.
Capture: HA723627, Mouse IL-27A p28 Rabbit mAb [PSH14-33]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
RAW 264.7 cells were cultured for 48 hours and stimulated with 5 µg/ml LPS. The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are stimulated RAW 264.7 cell culture supernatant 100%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean IL-27A p28 concentration was to be 1,264 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant. -
![Interpolated concentrations of native IL-27A p28 in RAW 264.7 cell culture supernatant.<br /><br />Capture: <a href="/products/HA723624" style="font-weight: bold;text-decoration: underline;">HA723624</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-31]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />RAW2 64.7 were stimulated with 5 µg/ml LPS and incubated for 48 hours. The concentrations of IL-27A p28 were interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are LPS stimulated RAW 264.7 cell culture supernatant 50% and unstimulated RAW 264.7 cell culture supernatant 50%. The mean IL-27A p28 concentration was determined to be 2,074 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant and undetectable in the unstimulated RAW 264.7 cell culture supernatant.](https://storage.huabio.cn/huabio/productImg/HA723625_5.png?v=20260429162005)
Interpolated concentrations of native IL-27A p28 in RAW 264.7 cell culture supernatant.
Capture: HA723624, Mouse IL-27A p28 Rabbit mAb [PSH14-31]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
RAW2 64.7 were stimulated with 5 µg/ml LPS and incubated for 48 hours. The concentrations of IL-27A p28 were interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are LPS stimulated RAW 264.7 cell culture supernatant 50% and unstimulated RAW 264.7 cell culture supernatant 50%. The mean IL-27A p28 concentration was determined to be 2,074 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant and undetectable in the unstimulated RAW 264.7 cell culture supernatant. -
![Interpolated concentrations of native IL-27A p28 in RAW 264.7 cell culture supernatant.<br /><br />Capture: <a href="/products/HA723627" style="font-weight: bold;text-decoration: underline;">HA723627</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-33]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />RAW2 64.7 were stimulated with 5 µg/ml LPS and incubated for 48 hours. The concentrations of IL-27A p28 were interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are LPS stimulated RAW 264.7 cell culture supernatant 50% and unstimulated RAW 264.7 cell culture supernatant 50%. The mean IL-27A p28 concentration was determined to be 1,264 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant and undetectable in the unstimulated RAW 264.7 cell culture supernatant.](https://storage.huabio.cn/huabio/productImg/HA723625_6.png?v=20260429162005)
Interpolated concentrations of native IL-27A p28 in RAW 264.7 cell culture supernatant.
Capture: HA723627, Mouse IL-27A p28 Rabbit mAb [PSH14-33]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
RAW2 64.7 were stimulated with 5 µg/ml LPS and incubated for 48 hours. The concentrations of IL-27A p28 were interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are LPS stimulated RAW 264.7 cell culture supernatant 50% and unstimulated RAW 264.7 cell culture supernatant 50%. The mean IL-27A p28 concentration was determined to be 1,264 pg/ml in LPS stimulated RAW 264.7 cell culture supernatant and undetectable in the unstimulated RAW 264.7 cell culture supernatant. -
![Interpolated concentrations of spiked IL-27A p28 in human cell culture media samples.<br /><br />Capture: <a href="/products/HA723624" style="font-weight: bold;text-decoration: underline;">HA723624</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-31]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are as follows: cell culture media 50%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2).](https://storage.huabio.cn/huabio/productImg/HA723625_7.png?v=20260429162005)
Interpolated concentrations of spiked IL-27A p28 in human cell culture media samples.
Capture: HA723624, Mouse IL-27A p28 Rabbit mAb [PSH14-31]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are as follows: cell culture media 50%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). -
![Interpolated concentrations of spiked IL-27A p28 in human cell culture media samples.<br /><br />Capture: <a href="/products/HA723627" style="font-weight: bold;text-decoration: underline;">HA723627</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-33]<br />Detector: <a href="/products/HA723625" style="font-weight: bold;text-decoration: underline;">HA723625</a>, Mouse IL-27A p28 Rabbit mAb [PSH14-32]<br /><br />The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are as follows: cell culture media 50%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2).](https://storage.huabio.cn/huabio/productImg/HA723625_8.png?v=20260429162005)
Interpolated concentrations of spiked IL-27A p28 in human cell culture media samples.
Capture: HA723627, Mouse IL-27A p28 Rabbit mAb [PSH14-33]
Detector: HA723625, Mouse IL-27A p28 Rabbit mAb [PSH14-32]
The concentrations of IL-27A p28 were measured in duplicates, interpolated from the IL-27A p28 standard curves and corrected for sample dilution. Undiluted samples are as follows: cell culture media 50%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2).
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"