CCL2 / MCP-1
HUABIO
catalog: HA500267
domestic rabbit polyclonal
reactivity: mouse
application: western blot, flow cytometry

Western blot analysis of CCL2 / MCP-1 on different lysates with Rabbit anti-CCL2 / MCP-1 antibody (HA500267) at 1/5,000 dilution. Lane 1: RAW264.7 cell lysate Lane 2: RAW264.7 treated with 100nM TPA overnight then 100ng/mL LPS for 7 hours add 1μg/mL BFA for last 3 hours cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 16 kDa Observed band size: 16 kDa Exposure time: 10 seconds; ECL: K1801; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA500267) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

Immunocytochemistry analysis of RAW264.7 cells untreated / treated with 100nM TPA overnight then 100ng/mL LPS for 7 hours add 1μg/mL BFA for last 3 hours labeling CCL2 / MCP-1 with Rabbit anti-CCL2 / MCP-1 antibody (HA500267) at 1/500 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-CCL2 / MCP-1 antibody (HA500267) at 1/500 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

Flow cytometric analysis of RAW264.7 cells untreated (left) / treated with 100nM TPA overnight then 100ng/mL LPS for 7 hours add 1μg/mL BFA for last 3 hours (right) labeling CCL2 / MCP-1. Cells were fixed and permeabilized. Then stained with the primary antibody (HA500267, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
quantity: 100μl
price: 330 USD
to the supplier
CCL2 / MCP-1
HUABIO
catalog: HA723691
domestic rabbit monoclonal (PSH12-44)
reactivity: mouse
application: western blot, flow cytometry

Western blot analysis of CCL2 / MCP-1 on different lysates with Rabbit anti-CCL2 / MCP-1 antibody (HA723691) at 1/2,000 dilution. Lane 1: RAW264.7 cell lysate Lane 2: RAW264.7 treated with 100ng/mL LPS for 4 hours add 1μg/mL BFA for3 hours cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 16 kDa Observed band size: 16 kDa Exposure time: 3 minutes; ECL: K1802; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA723691) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

Immunocytochemistry analysis of RAW264.7 cells untreated / treated with 100ng/mL LPS for 4 hours add 1μg/mL BFA for3 hours labeling CCL2 / MCP-1 with Rabbit anti-CCL2 / MCP-1 antibody (HA723691) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-CCL2 / MCP-1 antibody (HA723691) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

Flow cytometric analysis of RAW264.7 cells untreated (left) / treated with 100ng/mL LPS for 4 hours add 1μg/mL BFA for3 hours (right) labeling CCL2 / MCP-1. Cells were fixed and permeabilized. Then stained with the primary antibody (HA723691, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
quantity: 100μl
price: 385.00 USD
to the supplier
CCL2 / MCP-1
HUABIO
catalog: HA723979
domestic rabbit monoclonal (PSH18-16)
reactivity: mouse, rat
application: western blot, flow cytometry

Western blot analysis of CCL2 / MCP-1 on different lysates with Rabbit anti-CCL2 / MCP-1 antibody (HA723979) at 1/5,000 dilution. Lane 1: RAW264.7 cell lysate (20 µg/Lane) Lane 2: RAW264.7 treated with 100nM TPA overnight then treated with 100ng/mL LPS for 7 hours add 1μg/mL BFA for last 3 hours cell lysate (20 µg/Lane) Predicted band size: 16 kDa Observed band size: 20 kDa Exposure time: 3 minutes; ECL: K1802; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA723979) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

Western blot analysis of CCL2 / MCP-1 on different lysates with Rabbit anti-CCL2 / MCP-1 antibody (HA723979) at 1/2,000 dilution. Lane 1: NR8383 cell lysate (40 µg/Lane) Lane 2: NR8383 treated with 100nM TPA overnight then treated with 100ng/mL LPS for 7 hours add 1μg/mL BFA for last 3 hours cell lysate (40 µg/Lane) Predicted band size: 16 kDa Observed band size: 20 kDa Exposure time: 3 minutes; ECL: K1802; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA723979) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

Immunocytochemistry analysis of RAW264.7 cells untreated / treated with 100nM TPA overnight then treated with 100ng/mL LPS for 7 hours add 1μg/mL BFA for last 3 hours labeling CCL2 / MCP-1 with Rabbit anti-CCL2 / MCP-1 antibody (HA723979) at 1/250 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-CCL2 / MCP-1 antibody (HA723979) at 1/250 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
quantity: 100μl
price: 385.00 USD
to the supplier
Mouse CCL2 / MCP-1
HUABIO
catalog: HA725040
domestic rabbit monoclonal (PSH12-44)
reactivity: mouse
application: ELISA

Sandwich ELISA analysis of Mouse CCL2 matched pair antibodies Capture: HA725040, Mouse CCL2 Rabbit mAb [PSH12-44] Detector: HA725041, Mouse CCL2 Rabbit mAb [PSH12-45] Elisa assay was performed by coating wells of a 96-well plate with 50 µl per well of capture antibody (HA725040) 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 CCL2 protein (HA210775) starting from 2,000 pg/ml to 0 pg/ml and detect antibody (HA725041, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 50 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 CCL2 in J774A.1 cell culture supernatant. Capture: HA725040, Mouse CCL2 Rabbit mAb [PSH12-44] Detector: HA725041, Mouse CCL2 Rabbit mAb [PSH12-45] J774A.1 were stimulated with 20 ng/ml IFN-γ and 1 μg/ml LPS incubated for 1 day. The concentrations of CCL2 were measured in duplicate and interpolated from the CCL2 standard curves. Undiluted samples are IFN-γ and LPS stimulated J774A.1 cell culture supernatant 1.56% and unstimulated J774A.1 cell culture supernatant 50%. The mean CCL2 concentration was determined to be 13,358 pg/ml in IFN-γ and LPS stimulated J774A.1 cell culture supernatant and 1,679 pg/ml in the unstimulated J774A.1 cell culture supernatant.
quantity: 100μl
price: 649.00 USD
to the supplier
Mouse CCL2 / MCP-1
HUABIO
catalog: HA725041
domestic rabbit monoclonal (PSH12-45)
reactivity: mouse
application: ELISA

Sandwich ELISA analysis of Mouse CCL2 matched pair antibodies Capture: HA725040, Mouse CCL2 Rabbit mAb [PSH12-44] Detector: HA725041, Mouse CCL2 Rabbit mAb [PSH12-45] Elisa assay was performed by coating wells of a 96-well plate with 50 µl per well of capture antibody (HA725040) 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 CCL2 protein (HA210775) starting from 2,000 pg/ml to 0 pg/ml and detect antibody (HA725041, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 50 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 CCL2 in J774A.1 cell culture supernatant. Capture: HA725040, Mouse CCL2 Rabbit mAb [PSH12-44] Detector: HA725041, Mouse CCL2 Rabbit mAb [PSH12-45] J774A.1 were stimulated with 20 ng/ml IFN-γ and 1 μg/ml LPS incubated for 1 day. The concentrations of CCL2 were measured in duplicate and interpolated from the CCL2 standard curves. Undiluted samples are IFN-γ and LPS stimulated J774A.1 cell culture supernatant 1.56% and unstimulated J774A.1 cell culture supernatant 50%. The mean CCL2 concentration was determined to be 13,358 pg/ml in IFN-γ and LPS stimulated J774A.1 cell culture supernatant and 1,679 pg/ml in the unstimulated J774A.1 cell culture supernatant.
quantity: 100μl
price: 649.00 USD
to the supplier
Mouse CCL2 / MCP-1
HUABIO
catalog: HA725042B
domestic rabbit monoclonal (PSH12-45)
reactivity: mouse
conjugate: biotin
application: ELISA

Sandwich ELISA analysis of Mouse CCL2 matched pair antibodies Capture: HA725040, Mouse CCL2 Rabbit mAb [PSH12-44] Detector: HA725041, Mouse CCL2 Rabbit mAb [PSH12-45] Elisa assay was performed by coating wells of a 96-well plate with 50 µl per well of capture antibody (HA725040) 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 CCL2 protein (HA210775) starting from 2,000 pg/ml to 0 pg/ml and detect antibody (HA725041, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 50 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 CCL2 in J774A.1 cell culture supernatant. Capture: HA725040, Mouse CCL2 Rabbit mAb [PSH12-44] Detector: HA725041, Mouse CCL2 Rabbit mAb [PSH12-45] J774A.1 were stimulated with 20 ng/ml IFN-γ and 1 μg/ml LPS incubated for 1 day. The concentrations of CCL2 were measured in duplicate and interpolated from the CCL2 standard curves. Undiluted samples are IFN-γ and LPS stimulated J774A.1 cell culture supernatant 1.56% and unstimulated J774A.1 cell culture supernatant 50%. The mean CCL2 concentration was determined to be 13,358 pg/ml in IFN-γ and LPS stimulated J774A.1 cell culture supernatant and 1,679 pg/ml in the unstimulated J774A.1 cell culture supernatant.
quantity: 100μl
price: 409.00 USD
to the supplier
CCL2 / MCP-1
HUABIO
catalog: HA751533
domestic rabbit monoclonal (PSH12-44)
reactivity: mouse
application: western blot, flow cytometry

Western blot analysis of CCL2 / MCP-1 on different lysates with Rabbit anti-CCL2 / MCP-1 antibody (HA751533) at 1/2,000 dilution. Lane 1: RAW264.7 cell lysate Lane 2: RAW264.7 treated with 100ng/mL LPS for 4 hours add 1μg/mL BFA for3 hours cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 16 kDa Observed band size: 16 kDa Exposure time: 3 minutes; ECL: K1802; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA751533) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

Immunocytochemistry analysis of RAW264.7 cells untreated / treated with 100ng/mL LPS for 4 hours add 1μg/mL BFA for3 hours labeling CCL2 / MCP-1 with Rabbit anti-CCL2 / MCP-1 antibody (HA751533) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-CCL2 / MCP-1 antibody (HA751533) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (HA601187, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

Flow cytometric analysis of RAW264.7 cells untreated (left) / treated with 100ng/mL LPS for 4 hours add 1μg/mL BFA for3 hours (right) labeling CCL2 / MCP-1. Cells were fixed and permeabilized. Then stained with the primary antibody (HA751533, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
quantity: 100μl
price: 385.00 USD
to the supplier