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SouthernBiotech igg4
Indirect immunofluorescence on sections of monkey retina. The fluorescence observed is identified by a black arrow. (A) Patient 4 <t>(IgG4);</t> (B) Patient 1 (IgG4); (C) Patient 3 (IgG1); (D) Patient 5 (IgG4); (E) Patient 2 (IgG1); (F) Patient 1 (IgG4) after immunoadsorption of IgLON5 antibodies; (G) Control with macular edema (IgG1); (H) Control with anti-Hu encephalitis (IgG1); (I) Control with CAR syndrome (IgG4). The different layers of the retina are identified by their initials: pigment epithelium (pe), photoreceptor layer (pr), outer grain layer (og), outer plexiform layer (op), inner grain layer (ig), inner plexiform layer (ip), ganglion cell layer (gc), nerve fibre layer (nf).
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1) Product Images from "Anti-IgLON5 encephalitis is associated with anti-retinal immunological reactivity without retinal alteration"

Article Title: Anti-IgLON5 encephalitis is associated with anti-retinal immunological reactivity without retinal alteration

Journal: Journal of Translational Autoimmunity

doi: 10.1016/j.jtauto.2026.100359

Indirect immunofluorescence on sections of monkey retina. The fluorescence observed is identified by a black arrow. (A) Patient 4 (IgG4); (B) Patient 1 (IgG4); (C) Patient 3 (IgG1); (D) Patient 5 (IgG4); (E) Patient 2 (IgG1); (F) Patient 1 (IgG4) after immunoadsorption of IgLON5 antibodies; (G) Control with macular edema (IgG1); (H) Control with anti-Hu encephalitis (IgG1); (I) Control with CAR syndrome (IgG4). The different layers of the retina are identified by their initials: pigment epithelium (pe), photoreceptor layer (pr), outer grain layer (og), outer plexiform layer (op), inner grain layer (ig), inner plexiform layer (ip), ganglion cell layer (gc), nerve fibre layer (nf).
Figure Legend Snippet: Indirect immunofluorescence on sections of monkey retina. The fluorescence observed is identified by a black arrow. (A) Patient 4 (IgG4); (B) Patient 1 (IgG4); (C) Patient 3 (IgG1); (D) Patient 5 (IgG4); (E) Patient 2 (IgG1); (F) Patient 1 (IgG4) after immunoadsorption of IgLON5 antibodies; (G) Control with macular edema (IgG1); (H) Control with anti-Hu encephalitis (IgG1); (I) Control with CAR syndrome (IgG4). The different layers of the retina are identified by their initials: pigment epithelium (pe), photoreceptor layer (pr), outer grain layer (og), outer plexiform layer (op), inner grain layer (ig), inner plexiform layer (ip), ganglion cell layer (gc), nerve fibre layer (nf).

Techniques Used: Immunofluorescence, Fluorescence, Control

Related Articles

Bioprocessing:

Article Title:
Article Snippet: 3 nature portfolio | rep orting sum m ary M arch 2021 Materials & experimental systems n/a Involved in the study Antibodies Eukaryotic cell lines Palaeontology and archaeology Animals and other organisms Clinical data Dual use research of concern Methods n/a Involved in the study ChIP-seq Flow cytometry MRI-based neuroimaging Antibodies Antibodies used Validation Eukaryotic cell lines Policy information about cell lines and Sex and Gender in Research Cell line source(s) Authentication Mycoplasma contamination Commonly misidentified lines (See ICLAC register) Animals and other research organisms Policy information about studies involving animals; ARRIVE guidelines recommended for reporting animal research, and Sex and Gender in Research Laboratory animals Wild animals Reporting on sex Field-collected samples For immunolocalization in human biopsy samples, the following antibodies were used: collagen IV (goat, 1:400, Southern Biotech 1340-01), human IgG (Cy2 or Cy3 donkey anti-human IgG, 1:200; Jackson ImmunoResearch Laboratories ), C2 (mouse, 1:10; Santa Cruz, sc373809), C4b (rabbit, 1:500; Abcam ab181241), CFB (rabbit, 1:20; Proteintech 10170-1-AP), C3b (mouse, 1:1000; Abcam ab11871), C1q (rabbit, 1:1500; Dako A0136), C1q (goat serum, 1:400; Complement Technology A200), MBL (rabbit, 1:800; Abcam ab190834). .. For the localization of human IgG subclasses, monoclonal antibodies against IgG1 (mouse, 1:100, SouthernBiotech, 9052-01, clone no. 4E3), IgG2 (mouse, 1:40000, SouthernBiotech, 9080-01, clone no. HP6014), IgG3 (mouse, 1:1000, SouthernBiotech, 9210-01, clone no. HP6050), and IgG4 (mouse, 1:4000, SouthernBiotech, 9200-09, clone no. HP6025) were used. .. For immunolocalization in mice, the following antibodies were used: nephrin (guinea pig, 1:200; Acris Antibodies BP5030), neph1 (guinea pig, 1:200; kindly provided by Florian Grahammer), laminin (rabbit, 1:1000; Sigma-Aldrich L9393), WGA-rhodamin (1:400; Vector-Laboratories), THSD7A (goat, 1:200; Santa Cruz Biotechnology sc163455 or rabbit, 1:200; Sigma-Aldrich HPA000923), C1q (goat serum, 1:400; Complement Technology A200), C3 (FITC goat anti-C3, 1:100; Cappel 55500), C4d (rabbit, 1:50; Hycultec HP8033), C5b-9 (rabbit, 1:200; Abcam ab55811), CFB (goat, 1:50; Complement Technology A235), CFH (goat, 1:100; Complement Technology A237), MBL (rabbit, 1:800; Abcam ab190834), murine IgG (Cy2 donkey anti-mouse IgG H+L, 1:200; Jackson ImmunoResearch Laboratories), murine IgG subclasses (IgG1, IgG2a, IgG2b, IgG3) (goat, 1:5000; Rockland 610-101-040, 610-101-041, 610-101-042, 610-101-043, respectively), synaptopodin (guinea pig, 1:200; Synaptic Systems 163004 or rabbit, 1:400; Santa Cruz 50459), DACH-1 (rabbit, 1:100; Sigma-Aldrich HPA012672), 8-oxoguanine (goat, 1:600; Abcam ab10802).

Incubation:

Article Title: Application of machine learning algorithms to identify serological predictors of COVID-19 severity and outcomes.
Article Snippet: .. Plateswere incubated for 2 h atRT,washed, and50 μLof anti-humanHRP IgG (1:5000, #A18823, Invitrogen, Thermo Fisher Scientific), IgA (1:5000, #A18787, Invitrogen, Thermo Fisher Scientific), IgG1 (1:4000, #9054-05, Southern Biotech), IgG2 (1:4000, #9060-05, Southern Biotech), IgG3 (1:4000, #921005, Southern Biotech) or IgG4 (1:8000, #9200-05, Southern Biotech) secondary antibodywas added. .. After 1 h incubation at RT, plates werewashed, and 100 μL of Sigmafast OPD (o-phenylenediamine dihydrochloride) solution (MilliporeSigma) was added.

Article Title: Application of machine learning algorithms to identify serological predictors of COVID-19 severity and outcomes.
Article Snippet: .. Plateswere incubated for 2 h atRT,washed, and50 μLof anti-humanHRP IgG (1:5000, #A18823, Invitrogen, Thermo Fisher Scientific), IgA (1:5000, #A18787, Invitrogen, Thermo Fisher Scientific), IgG1 (1:4000, #9054-05, Southern Biotech), IgG2 (1:4000, #9060-05, Southern Biotech), IgG3 (1:4000, #9210- 05, Southern Biotech) or IgG4 (1:8000, #9200-05, Southern Biotech) secondary antibodywas added. .. After 1 h incubation at RT, plates werewashed, and 100 μL of Sigmafast OPD (o-phenylenediamine dihydrochloride) solution (MilliporeSigma) was added.

Article Title: Integrated serological surveillance of communicable diseases in the Paraguayan Chaco, 2019
Article Snippet: .. For detection, samples were incubated for 45 minutes with a mixture of biotinylated mouse anti-human IgG (50 ng/well) and IgG4 (40 ng/well) (Southern Biotech, Birmingham, AL, USA), and then 30 minutes with R-phycoerythrin conjugated to streptavidin (250 ng/well) (Invitrogen, Waltham, MA, USA) as a fluorescent marker. ..

Clinical Proteomics:

Article Title: Anti-IgLON5 encephalitis is associated with anti-retinal immunological reactivity without retinal alteration
Article Snippet: .. The reactivity of the patients’ sera and/or CSF against the retina was evaluated retrospectively with frozen samples (−80°, EXPLAINEUR biobank) through an indirect immunofluorescence technique using sections of monkey retina (Ref. FA1172-1005, Euroimmun), detected with an FITC-labelled secondary antibody anti-human IgAGM (Euroimmun conjugate) or directed against IgA (ref. F0204, DAKO), IgM (ref. F0203, DAKO), IgG1 (ref. 9052-02, Southern Biotech) and IgG4 (ref. 9200-02, Southern Biotech). ..

Immunofluorescence:

Article Title: Anti-IgLON5 encephalitis is associated with anti-retinal immunological reactivity without retinal alteration
Article Snippet: .. The reactivity of the patients’ sera and/or CSF against the retina was evaluated retrospectively with frozen samples (−80°, EXPLAINEUR biobank) through an indirect immunofluorescence technique using sections of monkey retina (Ref. FA1172-1005, Euroimmun), detected with an FITC-labelled secondary antibody anti-human IgAGM (Euroimmun conjugate) or directed against IgA (ref. F0204, DAKO), IgM (ref. F0203, DAKO), IgG1 (ref. 9052-02, Southern Biotech) and IgG4 (ref. 9200-02, Southern Biotech). ..

Binding Assay:

Article Title: Anti-dengue virus antibodies that elicit complement-mediated lysis of Zika virion correlate with protection from severe dengue disease.
Article Snippet: After incubation, plates were washed using an automatic magnetic washer (Tecan Hydrospeed) with phosphate-buffered saline (PBS) containing 0.1% bovine serum albumin (BSA) and 0.02% Tween 20. .. Antigen-specific subclass/isotype binding was detected using PE-coupled anti-human detection antibodies (0.000625μg/μL) against IgA (SouthernBiotech #2050-09), IgM (SouthernBiotech #9020-09), total IgG (SouthernBiotech #9040-09), IgG1 (Southern-Biotech #9052-09), IgG2 (SouthernBiotech #9060-09), IgG3 (Southern-Biotech #9210-09), and IgG4 (SouthernBiotech #9200-09). .. Fluorescence was acquired using an iQue3 (Intellicyt) machine (Sartorius).

Marker:

Article Title: Integrated serological surveillance of communicable diseases in the Paraguayan Chaco, 2019
Article Snippet: .. For detection, samples were incubated for 45 minutes with a mixture of biotinylated mouse anti-human IgG (50 ng/well) and IgG4 (40 ng/well) (Southern Biotech, Birmingham, AL, USA), and then 30 minutes with R-phycoerythrin conjugated to streptavidin (250 ng/well) (Invitrogen, Waltham, MA, USA) as a fluorescent marker. ..



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Indirect immunofluorescence on sections of monkey retina. The fluorescence observed is identified by a black arrow. (A) Patient 4 <t>(IgG4);</t> (B) Patient 1 (IgG4); (C) Patient 3 (IgG1); (D) Patient 5 (IgG4); (E) Patient 2 (IgG1); (F) Patient 1 (IgG4) after immunoadsorption of IgLON5 antibodies; (G) Control with macular edema (IgG1); (H) Control with anti-Hu encephalitis (IgG1); (I) Control with CAR syndrome (IgG4). The different layers of the retina are identified by their initials: pigment epithelium (pe), photoreceptor layer (pr), outer grain layer (og), outer plexiform layer (op), inner grain layer (ig), inner plexiform layer (ip), ganglion cell layer (gc), nerve fibre layer (nf).
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Image Search Results


Indirect immunofluorescence on sections of monkey retina. The fluorescence observed is identified by a black arrow. (A) Patient 4 (IgG4); (B) Patient 1 (IgG4); (C) Patient 3 (IgG1); (D) Patient 5 (IgG4); (E) Patient 2 (IgG1); (F) Patient 1 (IgG4) after immunoadsorption of IgLON5 antibodies; (G) Control with macular edema (IgG1); (H) Control with anti-Hu encephalitis (IgG1); (I) Control with CAR syndrome (IgG4). The different layers of the retina are identified by their initials: pigment epithelium (pe), photoreceptor layer (pr), outer grain layer (og), outer plexiform layer (op), inner grain layer (ig), inner plexiform layer (ip), ganglion cell layer (gc), nerve fibre layer (nf).

Journal: Journal of Translational Autoimmunity

Article Title: Anti-IgLON5 encephalitis is associated with anti-retinal immunological reactivity without retinal alteration

doi: 10.1016/j.jtauto.2026.100359

Figure Lengend Snippet: Indirect immunofluorescence on sections of monkey retina. The fluorescence observed is identified by a black arrow. (A) Patient 4 (IgG4); (B) Patient 1 (IgG4); (C) Patient 3 (IgG1); (D) Patient 5 (IgG4); (E) Patient 2 (IgG1); (F) Patient 1 (IgG4) after immunoadsorption of IgLON5 antibodies; (G) Control with macular edema (IgG1); (H) Control with anti-Hu encephalitis (IgG1); (I) Control with CAR syndrome (IgG4). The different layers of the retina are identified by their initials: pigment epithelium (pe), photoreceptor layer (pr), outer grain layer (og), outer plexiform layer (op), inner grain layer (ig), inner plexiform layer (ip), ganglion cell layer (gc), nerve fibre layer (nf).

Article Snippet: The reactivity of the patients’ sera and/or CSF against the retina was evaluated retrospectively with frozen samples (−80°, EXPLAINEUR biobank) through an indirect immunofluorescence technique using sections of monkey retina (Ref. FA1172-1005, Euroimmun), detected with an FITC-labelled secondary antibody anti-human IgAGM (Euroimmun conjugate) or directed against IgA (ref. F0204, DAKO), IgM (ref. F0203, DAKO), IgG1 (ref. 9052-02, Southern Biotech) and IgG4 (ref. 9200-02, Southern Biotech).

Techniques: Immunofluorescence, Fluorescence, Control

( A ) Interleukin-2 (IL-2) and interferon gamma (IFN-γ) inhibition in CD3 + cells during allogeneic one-way MLR measured at day 2 and day 5, respectively, treated with 50 nM combination pharmacological inhibitors of TNF/TNFR targets of interest. Monotreatment groups included 50 nM of human IgG1. Cytokine inhibition was calculated as percent reduction from IgG1 control treatment. Ill denotes P <0.05 in student t-test for monotreatments vs. IgG1 control, # denotes P <0.05 in student t-tests for combination treatment groups vs. IgG1 controls and both constituent monotreatments. ( B ) Normalized IL-2 and IFN-γ expression in four promising combinations of TNF/TNFR inhibitors. ( C-D ) Proliferation in CD3 + cells during allogeneic one-way MLR measured at day 5 in the presence of combination pharmacological inhibition of TNF/TNFR targets of interest.* denotes P <0.05 in student t-test. Data from three unique stimulator-responder MLR pairs, mean ± SEM plotted. Large-molecule pharmacological TNF/TNFR inhibitors used: Adalimumab (abbr. Ada, α-TNF), Pateclizumab (α-LTA), Baminercept (abbr. Bam, LTβR decoy), Dapirolizumab (abbr. Dapiro, α-CD40L), Amlitelimab (abbr. Amlite, α-OX40L), CD30Li (α-CD30L), 4-1BB-Fc (4-1BB decoy), Quisovalimab (α-LIGHT), Duvakitug (α-TL1A), and GITRi (α-GITR).

Journal: bioRxiv

Article Title: Combination antagonism of TNF superfamily signaling for T cell immunosuppression

doi: 10.64898/2026.04.27.721101

Figure Lengend Snippet: ( A ) Interleukin-2 (IL-2) and interferon gamma (IFN-γ) inhibition in CD3 + cells during allogeneic one-way MLR measured at day 2 and day 5, respectively, treated with 50 nM combination pharmacological inhibitors of TNF/TNFR targets of interest. Monotreatment groups included 50 nM of human IgG1. Cytokine inhibition was calculated as percent reduction from IgG1 control treatment. Ill denotes P <0.05 in student t-test for monotreatments vs. IgG1 control, # denotes P <0.05 in student t-tests for combination treatment groups vs. IgG1 controls and both constituent monotreatments. ( B ) Normalized IL-2 and IFN-γ expression in four promising combinations of TNF/TNFR inhibitors. ( C-D ) Proliferation in CD3 + cells during allogeneic one-way MLR measured at day 5 in the presence of combination pharmacological inhibition of TNF/TNFR targets of interest.* denotes P <0.05 in student t-test. Data from three unique stimulator-responder MLR pairs, mean ± SEM plotted. Large-molecule pharmacological TNF/TNFR inhibitors used: Adalimumab (abbr. Ada, α-TNF), Pateclizumab (α-LTA), Baminercept (abbr. Bam, LTβR decoy), Dapirolizumab (abbr. Dapiro, α-CD40L), Amlitelimab (abbr. Amlite, α-OX40L), CD30Li (α-CD30L), 4-1BB-Fc (4-1BB decoy), Quisovalimab (α-LIGHT), Duvakitug (α-TL1A), and GITRi (α-GITR).

Article Snippet: Adalimumab (Cat. HY-P9908), Pateclizumab (Cat. HY-P990034), Baminercept (Cat. HY-P99459), Amlitelimab (Cat. HY-P99434), Dapirolizumab (Cat. HY-P99842A), Quisovalimab (Cat. HY-P99810), Duvakitug (Cat. HY-P99842A), human IgG1 (Cat. HY-P99001) and human IgG4 (Cat. HY-P99003) were purchased from MedChemExpress.

Techniques: Inhibition, Control, Expressing

( A-B ) Interleukin-2 (IL-2) and interferon gamma (IFN-γ) inhibition in CD3 + cells during allogeneic one-way MLR measured at day 2 and day 5, respectively, treated with 50 nM combination pharmacological inhibitors of TNF/TNFR targets of interest. Monotreatment groups included 50 nM of human IgG1. Cytokine expression normalized to IgG1 control treatment. * denotes P <0.05 in student t-test for monotreatments vs. IgG1 control. Data from three individual stimulator-responder MLR pairs, mean ± SEM plotted.

Journal: bioRxiv

Article Title: Combination antagonism of TNF superfamily signaling for T cell immunosuppression

doi: 10.64898/2026.04.27.721101

Figure Lengend Snippet: ( A-B ) Interleukin-2 (IL-2) and interferon gamma (IFN-γ) inhibition in CD3 + cells during allogeneic one-way MLR measured at day 2 and day 5, respectively, treated with 50 nM combination pharmacological inhibitors of TNF/TNFR targets of interest. Monotreatment groups included 50 nM of human IgG1. Cytokine expression normalized to IgG1 control treatment. * denotes P <0.05 in student t-test for monotreatments vs. IgG1 control. Data from three individual stimulator-responder MLR pairs, mean ± SEM plotted.

Article Snippet: Adalimumab (Cat. HY-P9908), Pateclizumab (Cat. HY-P990034), Baminercept (Cat. HY-P99459), Amlitelimab (Cat. HY-P99434), Dapirolizumab (Cat. HY-P99842A), Quisovalimab (Cat. HY-P99810), Duvakitug (Cat. HY-P99842A), human IgG1 (Cat. HY-P99001) and human IgG4 (Cat. HY-P99003) were purchased from MedChemExpress.

Techniques: Inhibition, Expressing, Control

Studies were performed to analyze whether blockade of TGF-α could inhibit chemotactic invasion and lymphatic metastasis of 4T1-EGFR cells. a Results from transwell invasion assays showing that Fepixnebart, a neutralizing antibody against TGFα (aTGFα), significantly inhibited chemotactic invasion of 4T1-EGFR cells toward svLEC-conditioned media. An isotype matched IgG antibody was used as control. For each condition, three fields per well were imaged and quantified across three independent experiments based on crystal violet-stained areas. Statistical analysis was performed using an unpaired two-tailed Student’s T-test. b Schematic overview of the in vivo experimental setup. 4T1 cells were orthotopically implanted into mice, followed by tail vein injection of Fepixnebart. Tumor-draining lymph nodes were collected for analysis 10 days later. c Bar graphs showing quantification of CK⁺ tumor cells in inguinal (ILN) and axillary (ALN) lymph nodes 10 days after orthotopic injection of 4T1-EGFR cells into mammary fat pads. Mice received a single intravenous injection of Fepixnebart (10 mg/kg; n = 9) or isotype IgG control ( n = 8) at the time of tumor cell implantation. Data are shown as mean ± SEM; statistical analysis by unpaired two-tailed Student’s t-test.

Journal: NPJ Breast Cancer

Article Title: TGF-α/EGFR-mediated lymphatic metastasis reveals a repositionable therapeutic target in breast cancer

doi: 10.1038/s41523-026-00941-0

Figure Lengend Snippet: Studies were performed to analyze whether blockade of TGF-α could inhibit chemotactic invasion and lymphatic metastasis of 4T1-EGFR cells. a Results from transwell invasion assays showing that Fepixnebart, a neutralizing antibody against TGFα (aTGFα), significantly inhibited chemotactic invasion of 4T1-EGFR cells toward svLEC-conditioned media. An isotype matched IgG antibody was used as control. For each condition, three fields per well were imaged and quantified across three independent experiments based on crystal violet-stained areas. Statistical analysis was performed using an unpaired two-tailed Student’s T-test. b Schematic overview of the in vivo experimental setup. 4T1 cells were orthotopically implanted into mice, followed by tail vein injection of Fepixnebart. Tumor-draining lymph nodes were collected for analysis 10 days later. c Bar graphs showing quantification of CK⁺ tumor cells in inguinal (ILN) and axillary (ALN) lymph nodes 10 days after orthotopic injection of 4T1-EGFR cells into mammary fat pads. Mice received a single intravenous injection of Fepixnebart (10 mg/kg; n = 9) or isotype IgG control ( n = 8) at the time of tumor cell implantation. Data are shown as mean ± SEM; statistical analysis by unpaired two-tailed Student’s t-test.

Article Snippet: Simultaneously, mice received a single intravenous dose of Fepixnebart (10 mg/kg) or an isotype-matched human IgG4 control antibody (HY-P99003, MedChemExpress).

Techniques: Control, Staining, Two Tailed Test, In Vivo, Injection