Antibody data
- Antibody Data
- Antigen structure
- References [3]
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- Validations
- Other assay [1]
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- Product number
- AHC7129 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- IL-12 p70 Monoclonal Antibody (A25C4B6), Biotin
- Antibody type
- Monoclonal
- Antigen
- Recombinant full-length protein
- Description
- This product is recommended as a detection antibody in Sandwich ELISA applications.
- Conjugate
- Biotin
- Antibody clone number
- A25C4B6
- Concentration
- 0.5 mg/mL
Submitted references Pro-inflammatory monocyte profile in patients with major depressive disorder and suicide behaviour and how ketamine induces anti-inflammatory M2 macrophages by NMDAR and mTOR.
DC-SIGN, but not sDC-SIGN, can modulate IL-2 production from PMA- and anti-CD3-stimulated primary human CD4 T cells.
Synthetic TLR agonists reveal functional differences between human TLR7 and TLR8.
Nowak W, Grendas LN, Sanmarco LM, Estecho IG, Arena ÁR, Eberhardt N, Rodante DE, Aoki MP, Daray FM, Carrera Silva EA, Errasti AE
EBioMedicine 2019 Dec;50:290-305
EBioMedicine 2019 Dec;50:290-305
DC-SIGN, but not sDC-SIGN, can modulate IL-2 production from PMA- and anti-CD3-stimulated primary human CD4 T cells.
Martinez O, Brackenridge S, El-Idrissi Mel-A, Prabhakar BS
International immunology 2005 Jun;17(6):769-78
International immunology 2005 Jun;17(6):769-78
Synthetic TLR agonists reveal functional differences between human TLR7 and TLR8.
Gorden KB, Gorski KS, Gibson SJ, Kedl RM, Kieper WC, Qiu X, Tomai MA, Alkan SS, Vasilakos JP
Journal of immunology (Baltimore, Md. : 1950) 2005 Feb 1;174(3):1259-68
Journal of immunology (Baltimore, Md. : 1950) 2005 Feb 1;174(3):1259-68
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Supportive validation
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- Invitrogen Antibodies (provider)
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- Experimental details
- Fig. 1 Increased plasma levels of IL-12 and IL-6 correlate with increased non-classical CD16 bright CD14 neg monocytes as well as with increased activation of classical CD16 neg CD14 bright monocytes in patients with MDD and suicide behaviour. Plasma levels of (a) IL-12p70 and (b) IL-6 in patients with MDD (n=33) and healthy controls (n=20) as determined by ELISA. Significant differences between patients with MDD and healthy controls were calculated using a 2-tailed Mann-Whitney test (** p < 0.01). (c) Representative dot plots, after gating in mononuclear CD11b + cells, showing the frequency of the three monocyte subsets based on CD14 vs. CD16 expression level in healthy controls and patients with MDD. Detailed gaiting strategy is shown in Supplementary Fig. S1. (d) The three monocytes subset are depicted as classical CD16 neg CD14 bright (blue), non-classical CD16 bright CD14 neg (green) and intermediate CD16 + CD14 + (red) for further analysis. Independent data are graphed in (e-g) showing decreased percentages of classical CD16 neg CD14 bright monocytes alongside an increased percentage of non-classical CD16brightCD14neg monocytes in peripheral blood of patients with MDD. The frequency of the three subpopulations of monocytes from the cohort of patients with MDD was also segregated based on IL-6 and IL-12 plasma levels. The threshold for high cytokine level was set as the mean value plus 1 SD of control group. One-way ANOVA test was performed (** p < 0.01; ns p > 0.05). (h
- Conjugate
- Biotin