IL-4 Antibodies for Flow Cytometry - Antibody Resource Page

387 matching IL-4 antibodies for Flow Cytometry after applying filters

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Supplier data
Bio-Rad (formerly AbD Serotec) MCA1304G IL-4 antibody, MCA1304G, Bio-Rad (formerly AbD Serotec) .

Rat Mono [BVD4-1D11], 500 ug
Mo
ELISA, FACS, IHC-F, WB

IL-4 antibody, MCA1304G, Bio-Rad (formerly AbD Serotec) , Enzyme Linked Immunosorbent Assay image

ELISA,

IL-4 antibody, MCA1304G, Bio-Rad (formerly AbD Serotec) , Immunohistochemistry frozen image

IHC-F,

IL-4 antibody, MCA1304G, Bio-Rad (formerly AbD Serotec) , Western Blot image

Supplier data
Bio-Rad (formerly AbD Serotec) MCA1525 IL-4 antibody, MCA1525, Bio-Rad (formerly AbD Serotec) .

Rat Mono [MP4-25D2], 500 ug
Hu, Pr
ELISA, FACS, IHC-F, WB

IL-4 antibody, MCA1525, Bio-Rad (formerly AbD Serotec) , Enzyme Linked Immunosorbent Assay image

ELISA,

IL-4 antibody, MCA1525, Bio-Rad (formerly AbD Serotec) , Immunohistochemistry frozen image

IHC-F,

IL-4 antibody, MCA1525, Bio-Rad (formerly AbD Serotec) , Western Blot image

Supplier data
Bio-Rad (formerly AbD Serotec) MCA1820F

IL-4 antibody, MCA1820F, Bio-Rad (formerly AbD Serotec) . <strong>Published customer image:</strong> <br>Mouse anti Bovine interleukin-4 antibody, clone CC303 used for the identification of interferonγ expressing dog lymphocytes by flow cytometry.<br><strong>Image caption:</strong><br>Representative dot plots illustrating the analysis of intracellular cytokine profile in T-cell subsets. (A) Pseudocolor plot distribution of short-term in vitro cultured (control or SLA-Ag stimulated) canine whole blood sample according to cell size (Forward scatter

Mouse Mono [CC303], 100 ug
Bv, Cn, Eq, Gt, Po, Sh
FACS

Supplier data
Bio-Rad (formerly AbD Serotec) MCA1820PE

IL-4 antibody, MCA1820PE, Bio-Rad (formerly AbD Serotec) . <strong>Published customer image:</strong> <br>Mouse anti Bovine interleukin-4 antibody, clone CC303 used for the identification of interferonγ expressing dog lymphocytes by flow cytometry.<br><strong>Image caption:</strong><br>Representative dot plots illustrating the analysis of intracellular cytokine profile in T-cell subsets. (A) Pseudocolor plot distribution of short-term in vitro cultured (control or SLA-Ag stimulated) canine whole blood sample according to cell size (Forward scatter

Mouse Mono [CC303], 100 Test
Bv, Cn, Eq, Gt, Po, Sh
FACS

(1)

1 review

Supplier data
Origene AM39038RP-N IL-4 antibody, AM39038RP-N, Origene.

Mouse Mono [Clone 8F-12], 100 Test
Hu
FACS

Supplier data
Origene AM39038PU-N IL-4 antibody, AM39038PU-N, Origene.

Mouse Mono [Clone 8F-12], 1 ml
Hu
FACS

Supplier data
Lifespan Biosciences LS-C165210 IL-4 antibody, LS-C165210, Lifespan Biosciences. IL4 Antibody flow cytometry of WiDr cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

IL-4 antibody, LS-C165210, Lifespan Biosciences. IL4 Antibody flow cytometry of WiDr cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Rabbit Poly, 100 ug
Hu, Mo
FACS, IHC-F, IHC-P, WB

IL-4 antibody, LS-C165210, Lifespan Biosciences, Immunohistochemistry frozen image

IHC-F,

IL-4 antibody, LS-C165210, Lifespan Biosciences, Immunohistochemistry paraffin image

IHC-P,

IL-4 antibody, LS-C165210, Lifespan Biosciences, Western Blot image

Supplier data
BioLegend 500835 IL-4 antibody, 500835, BioLegend.

Rat Mono [MP4-25D2], 25 Test
Hu, Po, Pr
FACS

Supplier data
BioLegend 504125 IL-4 antibody, 504125, BioLegend. PMA+ionomycin-stimulated (6 hours, in presence of brefeldin A) Th2-polarized C57BL/6 T cells were surface stained with CD4 FITC, and then intracellularly stained with IL-4 ( clone 11B11) Brilliant Violet 605™ (top) or rat IgG1, κ Brilliant Violet 605™ isotype control (bottom).

IL-4 antibody, 504125, BioLegend. PMA+ionomycin-stimulated (6 hours, in presence of brefeldin A) Th2-polarized C57BL/6 T cells were surface stained with CD4 FITC, and then intracellularly stained with IL-4 ( clone 11B11) Brilliant Violet 605™ (top) or rat IgG1, κ Brilliant Violet 605™ isotype control (bottom).

Rat Mono [11B11], 125 ul
Mo
FACS

Supplier data
BioLegend 504126 IL-4 antibody, 504126, BioLegend. PMA+ionomycin-stimulated (6 hours, in presence of brefeldin A) Th2-polarized C57BL/6 T cells were surface stained with CD4 FITC, and then intracellularly stained with IL-4 ( clone 11B11) Brilliant Violet 605™ (top) or rat IgG1, κ Brilliant Violet 605™ isotype control (bottom).

IL-4 antibody, 504126, BioLegend. PMA+ionomycin-stimulated (6 hours, in presence of brefeldin A) Th2-polarized C57BL/6 T cells were surface stained with CD4 FITC, and then intracellularly stained with IL-4 ( clone 11B11) Brilliant Violet 605™ (top) or rat IgG1, κ Brilliant Violet 605™ isotype control (bottom).

Rat Mono [11B11], 50 ug
Mo
FACS

Supplier data
BioLegend 500836 IL-4 antibody, 500836, BioLegend.

Rat Mono [MP4-25D2], 100 Test
Hu, Po, Pr
FACS

Supplier data
BioLegend 504123 IL-4 antibody, 504123, BioLegend. Th2-polarized cells from C57BL/6 mouse T cells were stimulated with anti-CD3 and anti-CD28 for 6 hours (in presence of brefeldin A). The cells were then stained with CD3 FITC and subsequently fixed, permeabilized, and stained with IL-4 (clone 11B11) PerCP/Cy5.5 (top) or rat IgG1, κ PerCP/Cy5.5 isotype control (bottom).

IL-4 antibody, 504123, BioLegend. Th2-polarized cells from C57BL/6 mouse T cells were stimulated with anti-CD3 and anti-CD28 for 6 hours (in presence of brefeldin A). The cells were then stained with CD3 FITC and subsequently fixed, permeabilized, and stained with IL-4 (clone 11B11) PerCP/Cy5.5 (top) or rat IgG1, κ PerCP/Cy5.5 isotype control (bottom).

Rat Mono [11B11], 25 ug
Mo
FACS

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Supplier data
BioLegend 504120 IL-4 antibody, 504120, BioLegend. PMA+ionomycin-stimulated (6 hours, in presence of brefeldin A) Th2-polarized C57BL/6 T cells were surface stained with CD4 APC and then intracellularly stained with IL-4 ( clone 11B11) Brilliant Violet 421™ (top) or rat IgG1, κ Brilliant Violet 421™ isotype control (bottom).

IL-4 antibody, 504120, BioLegend. PMA+ionomycin-stimulated (6 hours, in presence of brefeldin A) Th2-polarized C57BL/6 T cells were surface stained with CD4 APC and then intracellularly stained with IL-4 ( clone 11B11) Brilliant Violet 421™ (top) or rat IgG1, κ Brilliant Violet 421™ isotype control (bottom).

Rat Mono [11B11], 500 ul
Mo
FACS

Supplier data
BioLegend 500834 IL-4 antibody, 500834, BioLegend. Human peripheral blood lymphocytes were stimulated with PMA + ionomycin for 6 hours (in the presence of monensin), surface stained with CD3 PE, fixed, permeabilized, and then stained with IL-4 (clone MP4-25D2) APC/Cy7 (top) or rat IgG1, κ APC/Cy7 isotype control (bottom).

IL-4 antibody, 500834, BioLegend. Human peripheral blood lymphocytes were stimulated with PMA + ionomycin for 6 hours (in the presence of monensin), surface stained with CD3 PE, fixed, permeabilized, and then stained with IL-4 (clone MP4-25D2) APC/Cy7 (top) or rat IgG1, κ APC/Cy7 isotype control (bottom).

Rat Mono [MP4-25D2], 100 Test
Hu
FACS

Supplier data
BioLegend 500833 IL-4 antibody, 500833, BioLegend. Human peripheral blood lymphocytes were stimulated with PMA + ionomycin for 6 hours (in the presence of monensin), surface stained with CD3 PE, fixed, permeabilized, and then stained with IL-4 (clone MP4-25D2) APC/Cy7 (top) or rat IgG1, κ APC/Cy7 isotype control (bottom).

IL-4 antibody, 500833, BioLegend. Human peripheral blood lymphocytes were stimulated with PMA + ionomycin for 6 hours (in the presence of monensin), surface stained with CD3 PE, fixed, permeabilized, and then stained with IL-4 (clone MP4-25D2) APC/Cy7 (top) or rat IgG1, κ APC/Cy7 isotype control (bottom).

Rat Mono [MP4-25D2], 25 Test
Hu
FACS

Supplier data
BioLegend 500827 IL-4 antibody, 500827, BioLegend. PMA+ ionomycin-stimulated human peripheral blood lymphocytes (6 hours, in the presence of monensin) were surface stained with CD3 APC, fixed, permeabilized and then stained with IL-4 (clone MP4-25D2) Brilliant Violet 605™ (top) or rat IgG1, κ Brilliant Violet 605™ isotype control (bottom).

IL-4 antibody, 500827, BioLegend. PMA<sup>+</sup> ionomycin-stimulated human peripheral blood lymphocytes (6 hours, in the presence of monensin) were surface stained with CD3 APC, fixed, permeabilized and then stained with IL-4 (clone MP4-25D2) Brilliant Violet 605™ (top) or rat IgG1, κ Brilliant Violet 605™ isotype control (bottom).

Rat Mono [MP4-25D2], 25 Test
GP, Hu, Pr
FACS

Supplier data
BioLegend 504124 IL-4 antibody, 504124, BioLegend. Th2-polarized cells from C57BL/6 mouse T cells were stimulated with anti-CD3 and anti-CD28 for 6 hours (in presence of brefeldin A). The cells were then stained with CD3 FITC and subsequently fixed, permeabilized, and stained with IL-4 (clone 11B11) PerCP/Cy5.5 (top) or rat IgG1, κ PerCP/Cy5.5 isotype control (bottom).

IL-4 antibody, 504124, BioLegend. Th2-polarized cells from C57BL/6 mouse T cells were stimulated with anti-CD3 and anti-CD28 for 6 hours (in presence of brefeldin A). The cells were then stained with CD3 FITC and subsequently fixed, permeabilized, and stained with IL-4 (clone 11B11) PerCP/Cy5.5 (top) or rat IgG1, κ PerCP/Cy5.5 isotype control (bottom).

Rat Mono [11B11], 100 ug
Mo
FACS

Supplier data
Invitrogen Antibodies PA5-25165 IL-4 antibody, PA5-25165, Invitrogen Antibodies. Flow cytometry analysis of WiDr cells using an IL4 polyclonal antibody (Product # PA5-25165) (right) compared to a negative control cell (left) at a dilution of 1:10-50, followed by a FITC-conjugated goat anti-rabbit antibody

IL-4 antibody, PA5-25165, Invitrogen Antibodies. Flow cytometry analysis of WiDr cells using an IL4 polyclonal antibody (Product # PA5-25165) (right) compared to a negative control cell (left) at a dilution of 1:10-50, followed by a FITC-conjugated goat anti-rabbit antibody

Rabbit Poly, 100 ug
Hu, Mo
FACS, IHC-F, IHC-P, WB

IL-4 antibody, PA5-25165, Invitrogen Antibodies, Immunohistochemistry frozen image

IHC-F,

IL-4 antibody, PA5-25165, Invitrogen Antibodies, Immunohistochemistry paraffin image

IHC-P,

IL-4 antibody, PA5-25165, Invitrogen Antibodies, Western Blot image

Supplier data
Invitrogen Antibodies 11-7042-82

IL-4 antibody, 11-7042-82, Invitrogen Antibodies. Mouse splenocytes were stimulated with ConA for 2 days, followed by Mouse IL-2 Recombinant Protein (Product # 14-8021-64) and Mouse IL-4 Recombinant Protein (Product # 14-8041-80) for 3 days, and re-stimulated with immobilized Anti-Mouse CD3 Functional Grade Purified (Product # 16-0032-82) and soluble Anti-Mouse CD28 Functional Grade Purified (Product # 16-0281-82) in the presence of Brefeldin A (Product # 00-4506-51) for 5 hours. Cells were surface stained with Anti-Mouse CD4 PE (Product # 12-0

Rat Mono [BVD6-24G2], 100 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 25-7041-80

IL-4 antibody, 25-7041-80, Invitrogen Antibodies. Mouse Th2-polarized splenocytes were unstimulated (left) or stimulated (right) with the Cell Stimulation Cocktail (plus protein transport inhibitors) (Product # 00-4975-03). The cells were intracellularly stained with Anti-Mouse CD4 FITC (Product # 11-0042-82) and 0.125 µg of Anti-Mouse IL-4 PE-Cyanine7 using the Intracellular Fixation & Permeabilization Buffer Set (Product # 88-8824-00) and protocol. Total viable cells, as determined by Fixable Viability Dye eFluor® 450 (Product # 65-

Rat Mono [11B11], 25 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 13-7042-85

IL-4 antibody, 13-7042-85, Invitrogen Antibodies. Staining of mouse splenocytes stimulated with ConA for 2 days, followed by IL-2 and IL-4 for 3 days, and restimulated with immobilized Anti-Mouse CD3 Functional Grade Purified (Product # 16-0031-82) and soluble Anti-Mouse CD28 Functional Grade Purified (Product # 16-0281-82) in the presence of Brefeldin A for 5 hours with Anti-Mouse CD4 PE (Product # 12-0041-82) and intracellularly stained with Anti-Mouse IL-4 FITC.

Rat Mono [BVD6-24G2], 500 ug
Mo
ELISA, FACS

ELISA

Supplier data
Invitrogen Antibodies 12-7041-82 IL-4 antibody, 12-7041-82, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor

IL-4 antibody, 12-7041-82, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor

Rat Mono [11B11], 100 ug
Mo
FACS

Supplier data
Cell Signaling Technology 12227S IL-4 antibody, 12227S, Cell Signaling Technology.

Rabbit Mono [D19A10], 100 ul
Hu
FACS, WB

IL-4 antibody, 12227S, Cell Signaling Technology, Western Blot image

Supplier data
ProSci 61-851 IL-4 antibody, 61-851, ProSci. Flow cytometric analysis of WiDr cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

IL-4 antibody, 61-851, ProSci. Flow cytometric analysis of WiDr cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Rabbit Poly, 400 ul
Hu, Mo
FACS, IHC-P, WB

IL-4 antibody, 61-851, ProSci, Immunohistochemistry paraffin image

IHC-P,

IL-4 antibody, 61-851, ProSci, Western Blot image

Supplier data
GeneTex GTX01492-07 IL-4 antibody, GTX01492-07, GeneTex. FACS analysis of human peripheral blood lymphocytes (with PMA and Ionomycin stimulation) using GTX01492-07 IL4 antibody [MP4-25D2] (APC). Right panel : co-stained with IL4 antibody [MP4-25D2] (APC) and Human CD3 antibody (PE) Left panel : co-stained with isotype control and Human CD3 antibody (PE) antibody amount : 0.0375 μg (5 μl)

IL-4 antibody, GTX01492-07, GeneTex. FACS analysis of human peripheral blood lymphocytes (with PMA and Ionomycin stimulation) using GTX01492-07 IL4 antibody [MP4-25D2] (APC).<br>Right panel : co-stained with IL4 antibody [MP4-25D2] (APC) and Human CD3 antibody (PE)<br>Left panel : co-stained with isotype control and Human CD3 antibody (PE)<br>antibody amount : 0.0375 μg (5 μl)

Rat Mono [MP4-25D2], 100 Test
Hu, Pr
FACS

Supplier data
Invitrogen Antibodies 13-7042-81

IL-4 antibody, 13-7042-81, Invitrogen Antibodies. Staining of mouse splenocytes stimulated with ConA for 2 days, followed by IL-2 and IL-4 for 3 days, and restimulated with immobilized Anti-Mouse CD3 Functional Grade Purified (Product # 16-0031-82) and soluble Anti-Mouse CD28 Functional Grade Purified (Product # 16-0281-82) in the presence of Brefeldin A for 5 hours with Anti-Mouse CD4 PE (Product # 12-0041-82) and intracellularly stained with Anti-Mouse IL-4 FITC.

Rat Mono [BVD6-24G2], 50 ug
Mo
ELISA, FACS

ELISA

Supplier data
Invitrogen Antibodies 25-7049-82 IL-4 antibody, 25-7049-82, Invitrogen Antibodies. Surface staining of normal human peripheral blood cells stimulated with PMA/Ionomycin in the presence of Brefeldin A with Anti-Human CD4 FITC (Product # 11-0048-42), followed by intracellular staining with Mouse IgG1 K Isotype Control PE-Cyanine7 (Product # 25-4714-80) (left) or Anti-Human IL-4 PE-Cyanine7 (right).

IL-4 antibody, 25-7049-82, Invitrogen Antibodies. Surface staining of normal human peripheral blood cells stimulated with PMA/Ionomycin in the presence of Brefeldin A with Anti-Human CD4 FITC (Product # 11-0048-42), followed by intracellular staining with Mouse IgG1 K Isotype Control PE-Cyanine7 (Product # 25-4714-80) (left) or Anti-Human IL-4 PE-Cyanine7 (right).

Mouse Mono [8D4-8], 100 ug
Hu
FACS

Supplier data
Invitrogen Antibodies 12-7049-41 IL-4 antibody, 12-7049-41, Invitrogen Antibodies. Normal human peripheral blood cells were stimulated with PMA and Ionomycin in the presence of brefeldin A for 6 hours. The cells were surface stained with Anti-Human CD3 FITC (Product # 11-0038-42) and intracellularly stained with Anti-Human IL-4 PE (right panel). Left panel demonstrates unlabelled antibody blocking control.

IL-4 antibody, 12-7049-41, Invitrogen Antibodies. Normal human peripheral blood cells were stimulated with PMA and Ionomycin in the presence of brefeldin A for 6 hours. The cells were surface stained with Anti-Human CD3 FITC (Product # 11-0038-42) and intracellularly stained with Anti-Human IL-4 PE (right panel). Left panel demonstrates unlabelled antibody blocking control.

Mouse Mono [8D4-8], 25 Test
Hu
FACS

Supplier data
Invitrogen Antibodies 53-7041-80

IL-4 antibody, 53-7041-80, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor® 780 (Product # 47-0041-82) and 1.0 µg of Rat IgG1 K Isotype Control Alexa Fluor® 488 (Product # 53-4301-80) (left) or 1.0 µg of Anti-Mouse IL-4 Alexa Fluor® 488 (right). Total viable cells, as determined by Fixable Viability Dye eFluor® 450, were used for analysis.

Rat Mono [11B11], 25 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 12-7049-42 IL-4 antibody, 12-7049-42, Invitrogen Antibodies. Normal human peripheral blood cells were stimulated with PMA and Ionomycin in the presence of brefeldin A for 6 hours. The cells were surface stained with Anti-Human CD3 FITC (Product # 11-0038-42) and intracellularly stained with Anti-Human IL-4 PE (right panel). Left panel demonstrates unlabelled antibody blocking control.

IL-4 antibody, 12-7049-42, Invitrogen Antibodies. Normal human peripheral blood cells were stimulated with PMA and Ionomycin in the presence of brefeldin A for 6 hours. The cells were surface stained with Anti-Human CD3 FITC (Product # 11-0038-42) and intracellularly stained with Anti-Human IL-4 PE (right panel). Left panel demonstrates unlabelled antibody blocking control.

Mouse Mono [8D4-8], 100 Test
Hu
FACS

Supplier data
Invitrogen Antibodies 46-7041-82

IL-4 antibody, 46-7041-82, Invitrogen Antibodies. Mouse Th2-polarized splenocytes were unstimulated (left) or restimulated (right) with the Cell Stimulation Cocktail (plus protein transport inhibitors) (Product # 00-4975-03). Cells were intracellularly stained with Anti-Mouse CD4 APC-eFluor® 780 (Product # 47-0041-82) and 0.06 µg of Anti-Mouse IL-4 PerCP-eFluor® 710. Total viable cells, as determined by Fixable Viability Dye eFluor® 450 (Product # 65-0863-14), were used for analysis.

Rat Mono [11B11], 100 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 11-7042-81

IL-4 antibody, 11-7042-81, Invitrogen Antibodies. Mouse splenocytes were stimulated with ConA for 2 days, followed by Mouse IL-2 Recombinant Protein (Product # 14-8021-64) and Mouse IL-4 Recombinant Protein (Product # 14-8041-80) for 3 days, and re-stimulated with immobilized Anti-Mouse CD3 Functional Grade Purified (Product # 16-0032-82) and soluble Anti-Mouse CD28 Functional Grade Purified (Product # 16-0281-82) in the presence of Brefeldin A (Product # 00-4506-51) for 5 hours. Cells were surface stained with Anti-Mouse CD4 PE (Product # 12-0

Rat Mono [BVD6-24G2], 50 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 17-7041-81

IL-4 antibody, 17-7041-81, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor® 780 (Product # 47-0041-82) and 0.125 µg of Rat IgG1 K Isotype Control APC (Product # 17-4301-82) (left) or 0.125 µg of Anti-Mouse IL-4 APC (right). Total viable cells, as determined by Fixable Viability Dye eFluor® 450 (Product # 65-0863-14) were used for analysis.

Rat Mono [11B11], 50 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 50-7045-82

IL-4 antibody, 50-7045-82, Invitrogen Antibodies. Rat splenocytes were cultured with Anti-Rat CD3 Functional Grade Purified (Product # 16-0030-85), Anti-Rat CD28 Functional Grade Purified (Product # 16-0280-81), Rat IL-2 Recombinant Protein (Product # 14-8020), and Rat IL-4 Recombinant Protein (Product # 14-8040) for 2 days followed by culture for an additional 3 days in Rat IL-2 and Rat IL-4 (right). The cells were then unstimulated (left) or stimulated (right) for 4 hours with the Cell Stimulation Cocktail (plus protein transport inhibitors)

Mouse Mono [OX81], 100 ug
Rt
FACS

Supplier data
Invitrogen Antibodies 25-7041-82

IL-4 antibody, 25-7041-82, Invitrogen Antibodies. Mouse Th2-polarized splenocytes were unstimulated (left) or stimulated (right) with the Cell Stimulation Cocktail (plus protein transport inhibitors) (Product # 00-4975-03). The cells were intracellularly stained with Anti-Mouse CD4 FITC (Product # 11-0042-82) and 0.125 µg of Anti-Mouse IL-4 PE-Cyanine7 using the Intracellular Fixation & Permeabilization Buffer Set (Product # 88-8824-00) and protocol. Total viable cells, as determined by Fixable Viability Dye eFluor® 450 (Product # 65-

Rat Mono [11B11], 100 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 50-7045-80

IL-4 antibody, 50-7045-80, Invitrogen Antibodies. Rat splenocytes were cultured with Anti-Rat CD3 Functional Grade Purified (Product # 16-0030-85), Anti-Rat CD28 Functional Grade Purified (Product # 16-0280-81), Rat IL-2 Recombinant Protein (Product # 14-8020), and Rat IL-4 Recombinant Protein (Product # 14-8040) for 2 days followed by culture for an additional 3 days in Rat IL-2 and Rat IL-4 (right). The cells were then unstimulated (left) or stimulated (right) for 4 hours with the Cell Stimulation Cocktail (plus protein transport inhibitors)

Mouse Mono [OX81], 25 ug
Rt
FACS

Supplier data
Invitrogen Antibodies 17-7041-82

IL-4 antibody, 17-7041-82, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor® 780 (Product # 47-0041-82) and 0.125 µg of Rat IgG1 K Isotype Control APC (Product # 17-4301-82) (left) or 0.125 µg of Anti-Mouse IL-4 APC (right). Total viable cells, as determined by Fixable Viability Dye eFluor® 450 (Product # 65-0863-14) were used for analysis.

Rat Mono [11B11], 100 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 12-7041-81 IL-4 antibody, 12-7041-81, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor

IL-4 antibody, 12-7041-81, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor

Rat Mono [11B11], 50 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 53-7041-82

IL-4 antibody, 53-7041-82, Invitrogen Antibodies. Intracellular staining of Th2-polarized mouse splenocytes with Anti-Mouse CD4 APC-eFluor® 780 (Product # 47-0041-82) and 1.0 µg of Rat IgG1 K Isotype Control Alexa Fluor® 488 (Product # 53-4301-80) (left) or 1.0 µg of Anti-Mouse IL-4 Alexa Fluor® 488 (right). Total viable cells, as determined by Fixable Viability Dye eFluor® 450, were used for analysis.

Rat Mono [11B11], 100 ug
Mo
FACS

Supplier data
Invitrogen Antibodies 46-7041-80

IL-4 antibody, 46-7041-80, Invitrogen Antibodies. Mouse Th2-polarized splenocytes were unstimulated (left) or restimulated (right) with the Cell Stimulation Cocktail (plus protein transport inhibitors) (Product # 00-4975-03). Cells were intracellularly stained with Anti-Mouse CD4 APC-eFluor® 780 (Product # 47-0041-82) and 0.06 µg of Anti-Mouse IL-4 PerCP-eFluor® 710. Total viable cells, as determined by Fixable Viability Dye eFluor® 450 (Product # 65-0863-14), were used for analysis.

Rat Mono [11B11], 25 ug
Mo
FACS

Supplier data
GeneTex GTX01492-08 IL-4 antibody, GTX01492-08, GeneTex. FACS analysis of human peripheral blood lymphocytes (with PMA and Ionomycin stimulation) using GTX01492-08 IL4 antibody [MP4-25D2] (PE). Right panel : co-stained with IL4 antibody [MP4-25D2] (PE) and Human CD3 antibody (APC) Left panel : co-stained with isotype control and Human CD3 antibody (APC) antibody amount : 0.125 μg (5 μl)

IL-4 antibody, GTX01492-08, GeneTex. FACS analysis of human peripheral blood lymphocytes (with PMA and Ionomycin stimulation) using GTX01492-08 IL4 antibody [MP4-25D2] (PE).<br>Right panel : co-stained with IL4 antibody [MP4-25D2] (PE) and Human CD3 antibody (APC)<br>Left panel : co-stained with isotype control and Human CD3 antibody (APC)<br>antibody amount : 0.125 μg (5 μl)

Rat Mono [MP4-25D2], 100 Test
Hu, Pr
FACS

Supplier data
Abbexa abx032452 IL-4 antibody, abx032452, Abbexa.

Rabbit Poly, 400 ul
Hu, Mo
FACS, WB

IL-4 antibody, abx032452, Abbexa, Western Blot image

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CD8	5.3%
CD25	5.1%
His tag	5.0%
ATP Binding Cassette Subfamily G Member 2 (Junior Blood Group)	5.0%
CD28	4.7%
PMP-22	4.6%
Interleukin 10	4.3%

Featured Research

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Bac	Bacteria
Bt	Bat
Bv	Bovine
Cel	C.Elegans
Cml	Camel
Cn	Canine
chem	Chemical
Ch	Chicken
Dk	Donkey
Dr	Drosophila
Du	Duck
Eq	Equine
Eu	Eukaryotes
Fe	Feline
Fi	Fish
Fr	Frog
Fu	Fungus
Gt	Goat
Gf	Goldfish
GP	Guinea Pig
Ha	Hamster
Hu	Human
Inv	Invertebrates
Llm	Llama
Mam	Mammals
Mo	Mouse
Pl	Plant
Po	Porcine
Pr	Primate
Pro	Prokaryotes
Rb	Rabbit
Rt	Rat
Sh	Sheep
Sq	Squirrel
Vert	Vertebrates
Vi	Virus
Xe	Xenopus
Yt	Yeast
Zf	Zebrafish

AP	Affinity purification
Bl	Blocking
ChIP	Chromatin Immunoprecipitation
DB	Dot Blot
EMSA	Electron Microscopy
ELISA	Enzyme Linked Immunosorbent Assay
FACS	Flow Cytometry
FA	Functional Assay
GS	Gel Shift
ICC	Immunocytochemistry
ID	Immunodiffusion
IF	Immunofluorescence
IHC-F	Immunohistochemistry frozen
IHC-P	Immunohistochemistry paraffin
IP	Immunoprecipitation
IVT	In vivo targeting
Neu	Neutralising
Pep-ELISA	Peptide ELISA
PLA	Proximity Ligation Assay
RIA	Radioimmunoassay
WB	Western Blot

387 matching IL-4 antibodies for Flow Cytometry from 35 suppliers

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1 Applications, 16 Species currently selected

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	ELISA	WB	FACS	IHC-P	IHC-F	ICC	IF	AP	Neu	IP	FA	IVT	Pep-ELISA	Bl	ChIP
Human	279	277	184	127	94	85	76	34	27	23	15	1	6		1
Mouse	207	162	255	82	86	71	72	21	28	23	17	11	4	2	2
Rat	71	99	39	28	23	50	54	6	5	3	5		7	5
Porcine	11	20	45	1	1	15	2		3	1
Primate	18	23	38	10	11	20	9		1	8
Canine	28	19	9	2	2	6	5		3
Bovine	21	4	22			2	2	1
Fish	20	19
Sheep	12		11
Rabbit	10	9		2	2	1	1		1
Goat	9		10
Bacteria	6		9	1	7				6
Guinea Pig	8	5	6	2	2	1	1
Equine	6	4	4			1	1
Feline	2	4							3
Chicken	2	3		1	1	2	1