human mspr antibody Search Results


90
Bio-Techne corporation human mspr/ron antibody
Human Mspr/Ron Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems goat polyclonal anti human msp antibody
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Goat Polyclonal Anti Human Msp Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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goat polyclonal anti human msp antibody - by Bioz Stars, 2026-08
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93
R&D Systems antibody against phospho ron
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Antibody Against Phospho Ron, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
antibody against phospho ron - by Bioz Stars, 2026-08
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92
R&D Systems goat anti mertk af691
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Goat Anti Mertk Af691, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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goat anti mertk af691 - by Bioz Stars, 2026-08
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R&D Systems human phospho mspr ron y1238 y1239 antibody
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Human Phospho Mspr Ron Y1238 Y1239 Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human phospho mspr ron y1238 y1239 antibody - by Bioz Stars, 2026-08
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93
R&D Systems human mspr antibody
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Human Mspr Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+mspr+antibody/pmc03721396-81-23-26?v=R%26D+Systems
Average 93 stars, based on 1 article reviews
human mspr antibody - by Bioz Stars, 2026-08
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85
R&D Systems goat anti human polyclonal
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Goat Anti Human Polyclonal, supplied by R&D Systems, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 85 stars, based on 1 article reviews
goat anti human polyclonal - by Bioz Stars, 2026-08
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90
Bio-Techne corporation human mspr/ron fluorescein-conjugated antibody
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Human Mspr/Ron Fluorescein Conjugated Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human mspr/ron fluorescein-conjugated antibody - by Bioz Stars, 2026-08
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90
R&D Systems goat polyclonal anti human ron antibody
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Goat Polyclonal Anti Human Ron Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+mspr+antibody/us10005848-969-0-5?v=R%26D+Systems
Average 90 stars, based on 1 article reviews
goat polyclonal anti human ron antibody - by Bioz Stars, 2026-08
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R&D Systems human ron activity
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Human Ron Activity, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ron activity - by Bioz Stars, 2026-08
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93
R&D Systems biotinylated polyclonal goat anti human msp
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Biotinylated Polyclonal Goat Anti Human Msp, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems pe conjugated goat anti human iggfc
Figure 1. Western blot performed with anti–macrophage-stimulating protein <t>(MSP)</t> antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP <t>polyclonal</t> Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.
Pe Conjugated Goat Anti Human Iggfc, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pe conjugated goat anti human iggfc - by Bioz Stars, 2026-08
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Image Search Results


Figure 1. Western blot performed with anti–macrophage-stimulating protein (MSP) antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP polyclonal Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.

Journal: Journal of the American Society of Nephrology : JASN

Article Title: Macrophage-stimulating protein is produced by tubular cells and activates mesangial cells.

doi: 10.1681/ASN.V133649

Figure Lengend Snippet: Figure 1. Western blot performed with anti–macrophage-stimulating protein (MSP) antibody (Ab) in culture supernatant of the human tubular cell line HK2, human mesangial cells (HMC), and the hepa- toma cell line HepG2. A 50 ml volume of supernatant was immuno- precipitated with anti-MSP polyclonal Ab adsorbed to protein A–sepharose 4B packed beads. Immunoprecipitates were washed with an ice-cold buffer, boiled after addition of 2 sample buffer, and the proteins were loaded onto 10% sodium dodecyl sulfate–polyacrylam- ide gel electrophoresis. Proteins were analyzed by Western blot that used a polyclonal anti-MSP Ab. The 85-kD bands represent mono- meric MSP (pro-MSP), and the 55-kD bands represent the -chain of dimeric (active) MSP. Both HK2 and HepG2 cells (used as controls) release pro-MSP that is cleaved into the dimeric form in the super- natant. No band is visible in the HMC lane.

Article Snippet: In some experiments, HMC were incubated with HK2 supernatant or with HK2 supernatant preincubated for 2 h with neutralizing goat polyclonal anti-human MSP antibody (Ab; 2 g/ml) (R&D Systems, Minneapolis, MN) without fresh medium.

Techniques: Western Blot, Nucleic Acid Electrophoresis