rabbit antiphosphorylated-jak2 (p-jak2, cat Search Results


90
Upstate Biotechnology Inc antiphosphorylated jak2
Antiphosphorylated Jak2, supplied by Upstate Biotechnology Inc, 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/result/antiphosphorylated jak2/product/Upstate Biotechnology Inc
Average 90 stars, based on 1 article reviews
antiphosphorylated jak2 - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

94
Cell Signaling Technology Inc jak 2
Jak 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/jak 2/product/Cell Signaling Technology Inc
Average 94 stars, based on 1 article reviews
jak 2 - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier

95
Cell Signaling Technology Inc rabbit monoclonal antiphosphorylated stat 3 ser727
Rabbit Monoclonal Antiphosphorylated Stat 3 Ser727, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit monoclonal antiphosphorylated stat 3 ser727/product/Cell Signaling Technology Inc
Average 95 stars, based on 1 article reviews
rabbit monoclonal antiphosphorylated stat 3 ser727 - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier

99
Cell Signaling Technology Inc rabbit monoclonal antiphosphorylated p38
Rabbit Monoclonal Antiphosphorylated P38, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit monoclonal antiphosphorylated p38/product/Cell Signaling Technology Inc
Average 99 stars, based on 1 article reviews
rabbit monoclonal antiphosphorylated p38 - by Bioz Stars, 2026-03
99/100 stars
  Buy from Supplier

95
Cell Signaling Technology Inc rabbit monoclonal antiphosphorylated stat 3 tyr705
Rabbit Monoclonal Antiphosphorylated Stat 3 Tyr705, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit monoclonal antiphosphorylated stat 3 tyr705/product/Cell Signaling Technology Inc
Average 95 stars, based on 1 article reviews
rabbit monoclonal antiphosphorylated stat 3 tyr705 - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier

97
Cell Signaling Technology Inc anti phosphorylated jak2 antibodies
Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and <t>p-Jak2</t> analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).
Anti Phosphorylated Jak2 Antibodies, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti phosphorylated jak2 antibodies/product/Cell Signaling Technology Inc
Average 97 stars, based on 1 article reviews
anti phosphorylated jak2 antibodies - by Bioz Stars, 2026-03
97/100 stars
  Buy from Supplier

95
Cell Signaling Technology Inc rabbit anti jak2
Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and <t>p-Jak2</t> analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).
Rabbit Anti Jak2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit anti jak2/product/Cell Signaling Technology Inc
Average 95 stars, based on 1 article reviews
rabbit anti jak2 - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier

90
Cell Signaling Technology Inc rabbit anti–c-myc
Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and <t>p-Jak2</t> analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).
Rabbit Anti–C Myc, supplied by Cell Signaling Technology Inc, 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/result/rabbit anti–c-myc/product/Cell Signaling Technology Inc
Average 90 stars, based on 1 article reviews
rabbit anti–c-myc - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

96
Cell Signaling Technology Inc jak2 tyr1007 1008
Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and <t>p-Jak2</t> analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).
Jak2 Tyr1007 1008, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/jak2 tyr1007 1008/product/Cell Signaling Technology Inc
Average 96 stars, based on 1 article reviews
jak2 tyr1007 1008 - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier

90
Promega anti-rabbit igg-hrp
Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and <t>p-Jak2</t> analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).
Anti Rabbit Igg Hrp, supplied by Promega, 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/result/anti-rabbit igg-hrp/product/Promega
Average 90 stars, based on 1 article reviews
anti-rabbit igg-hrp - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

90
Millipore anti-b-actin mab
Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and <t>p-Jak2</t> analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).
Anti B Actin Mab, supplied by Millipore, 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/result/anti-b-actin mab/product/Millipore
Average 90 stars, based on 1 article reviews
anti-b-actin mab - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

99
Cell Signaling Technology Inc antiphosphorylated akt
Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and <t>p-Jak2</t> analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).
Antiphosphorylated Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antiphosphorylated akt/product/Cell Signaling Technology Inc
Average 99 stars, based on 1 article reviews
antiphosphorylated akt - by Bioz Stars, 2026-03
99/100 stars
  Buy from Supplier

Image Search Results


Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and p-Jak2 analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).

Journal: Biochimica et biophysica acta

Article Title: Signaling pathways of cell proliferation are involved in the differential effect of erythropoietin and its carbamylated derivative.

doi: 10.1016/j.bbamcr.2013.04.006

Figure Lengend Snippet: Fig. 2. Expression of EpoR and βcR under different stages of cell differentiation. A) TF-1 and UT-7 cells were subjected to erythroid differentiation by 30 μM hemin during 48 h (H) while differentiation of neuronal SH-SY5Y cells was achieved by retinoic acid (10 μM RA, 4 days). Cell extracts were resolved by SDS-PAGE (T = 10%), electroblotted on a NC membrane and then immunodetected by chemiluminescence using specific antibodies. Each bar represents mean ± SEM of band density with respect to β-actin, used as control of sample loading. B) SH-SY5Y cell incubations with 250 ng/ml of either Epo (E) or cEpo (cE) for 10 min and p-Jak2 analyzed by flow cytometry. C) After 18 h without growth factors, TF-1 cells were incubated with 20 ng/ml Epo or 20 ng/ml cEpo during 10 min and p-Jak2 was detected. D) UT-7 cell cultures were incubated with 20 ng/ml of either Epo or cEpo (10 min) to determine Jak2 phosphorylation (p-Jak2). Each bar represents mean ± SEM. Significant differences of fluorescence intensity: **P b 0.01; * P b 0.05 (n = 3).

Article Snippet: Antiphosphorylated FOXO3a, anti-FOXO3a, and anti-phosphorylated Jak2 antibodies were from Cell Signaling Technology.

Techniques: Expressing, Cell Differentiation, SDS Page, Membrane, Control, Cytometry, Incubation, Phospho-proteomics