phospho trka Search Results


human phospho trka duoset ic elisa  (R&D Systems)
90
R&D Systems human phospho trka duoset ic elisa
Activation of <t>TrkA</t> in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) <t>ELISA</t> was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )
Human Phospho Trka Duoset Ic Elisa, 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/phospho+trka/pmc06899756-46-0-14?v=R%26D+Systems
Average 90 stars, based on 1 article reviews
human phospho trka duoset ic elisa - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier
anti phospho trka  (R&D Systems)
93
R&D Systems anti phospho trka
Activation of <t>TrkA</t> in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) <t>ELISA</t> was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )
Anti Phospho Trka, 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/phospho+trka/pmc12240581-35-12-13?v=R%26D+Systems
Average 93 stars, based on 1 article reviews
anti phospho trka - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier
anti phospho trka y785  (R&D Systems)
90
R&D Systems anti phospho trka y785
Activation of <t>TrkA</t> in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) <t>ELISA</t> was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )
Anti Phospho Trka Y785, 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/phospho+trka/pmc02903477-226-1-5?v=R%26D+Systems
Average 90 stars, based on 1 article reviews
anti phospho trka y785 - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier
anti-phospho-trka  (SignalChem)
90
SignalChem anti-phospho-trka
Activation of <t>TrkA</t> in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) <t>ELISA</t> was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )
Anti Phospho Trka, supplied by SignalChem, 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/phospho+trka/signalchem___n16-65r?v=SignalChem
Average 90 stars, based on 1 article reviews
anti-phospho-trka - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier
phospho trka duoset ic elisa detection kit  (R&D Systems)
93
R&D Systems phospho trka duoset ic elisa detection kit
Activation of <t>TrkA</t> in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) <t>ELISA</t> was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )
Phospho Trka Duoset Ic Elisa Detection Kit, 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/phospho+trka/pmc08442742-57-26-32?v=R%26D+Systems
Average 93 stars, based on 1 article reviews
phospho trka duoset ic elisa detection kit - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier
anti-phospho trka, tyr-490, antibody  (Westburg bv)
90
Westburg bv anti-phospho trka, tyr-490, antibody
Activation of <t>TrkA</t> in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) <t>ELISA</t> was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )
Anti Phospho Trka, Tyr 490, Antibody, supplied by Westburg bv, 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/phospho+trka/pm16914291-57-2-7?v=Westburg+bv
Average 90 stars, based on 1 article reviews
anti-phospho trka, tyr-490, antibody - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier
trka (phospho-tyr490) antibody (fitc)  (biorbyt)
N/A
Rabbit polyclonal antibody against phospho-TrkA (Tyr490) conjugated to FITC Isotype Note: IgG Host Note: Rabbit Conjugation Note: FITC Application Note: IF/ICC
   Buy from Supplier
trka (phospho-tyr701) antibody (fitc)  (biorbyt)
N/A
Rabbit polyclonal antibody against phospho-TrkA (Tyr701) conjugated to FITC Isotype Note: IgG Host Note: Rabbit Conjugation Note: FITC Reactivity Note: Human, Mouse, Rat Application Note: IF/ICC
   Buy from Supplier
phospho-trka (tyr490)/trkb (tyr516) rabbit mab  (Cell Signaling Technology Inc)
N/A
The family of Trk receptor tyrosine kinases consists of TrkA, TrkB, and TrkC. While the sequence of these family members is highly conserved, they are activated by different neurotrophins: TrkA by NGF, TrkB by BDNF
   Buy from Supplier
phospho-trka/b (tyr490/tyr516) antibody  (MedChemExpress)
N/A
Phospho-TrkA/B (Tyr490/Tyr516) Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 92 kDa (Observed band size: 140 kDa), targeting to Phospho-TrkA/B (Tyr490/Tyr516). It can be used for WB assays with tag free, in the
   Buy from Supplier
phospho-trka (tyr791) polyclonal antibody  (Thermo Fisher)
N/A
Phospho-TrkA (Tyr791) Polyclonal Antibody for DB
   Buy from Supplier
pathscan phospho-trka (tyr490) sandwich elisa kit  (Cell Signaling Technology Inc)
N/A
The family of Trk receptor tyrosine kinases consists of TrkA, TrkB, and TrkC. While the sequence of these family members is highly conserved, they are activated by different neurotrophins: TrkA by NGF, TrkB by BDNF
   Buy from Supplier

Image Search Results


Activation of TrkA in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) ELISA was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )

Journal: The European Journal of Neuroscience

Article Title: Identification of amino acid residues of nerve growth factor important for neurite outgrowth in human dorsal root ganglion neurons

doi: 10.1111/ejn.14513

Figure Lengend Snippet: Activation of TrkA in U2OS‐TrkA/p75‐SHC1 cells. Total chemiluminescent signal from all wavelengths was measured using reagents and recombinant cells from DiscoverX. The luminescent signal is proportional to the amount of interactions between TrkA and SHC1 or PLCγ1 present in each well. Normalized response of the interaction between TrkA and SHC1 in U2OS‐TrkA/p75‐SHC1 cells (a), or between TrkA and PLCγ1 in U2OS‐TrkA‐PLCγ1 cells (b) after 3 hr of treatment. Five (a) or four (b) independent biological repeats with four technical replicates were conducted. (c) ELISA was used to quantify direct phosphorylation of TrkA from three independent biological repeats after normalization to 100 ng/ml wild‐type NGF. Results are mean ± SEM , significant alterations compared with wild‐type NGF were found for 100 ng/ml and 300 ng/ml R100E (**** p < .0001), 30 ng/ml R100E (** p = .0016), 10 ng/ml R100E (** p = .0031), 300 ng/ml W99A (* p = .0363), 100 ng/ml K95A/Q96A (* p = .0185) and 300 ng/ml K95A/Q96A (*** p = .0006). Wild‐type NGF (black circles ●), NGF‐R100E (red squares ), NGF‐W99A (green diamonds ) or NGF‐K95A/Q96A (blue triangles )

Article Snippet: Human Phospho‐TrkA DuoSet IC ELISA and Phospho‐ERK1 (T202/Y204)/ERK2 (T185/Y187) DuoSet IC ELISA were from R&D Systems.

Techniques: Activation Assay, Recombinant, Enzyme-linked Immunosorbent Assay

Phospho‐ERK1/2 levels in cultured U2OS‐TrkA/p75‐SHC1 cells and PC12 cells investigated with ELISA. Analysis of pERK1/2 levels in U2OS‐TrkA cells (a) or PC12 cells (b) after NGF stimulation was performed with ELISA. There were significantly increased pERK1/2 levels for NGF‐R100E (*** p = .0005) compared with wild‐type NGF and significantly lower levels for vehicle‐treated U2OS‐TrkA/p75‐SHC1 cells (* p = .0121, a). In b, significantly lower pERK1/2 levels for vehicle‐treated PC12 cells compared with wild‐type NGF were found (* p = .0121). The results are presented as mean ± SEM from four independent biological repeats with one to twelve technical replicates

Journal: The European Journal of Neuroscience

Article Title: Identification of amino acid residues of nerve growth factor important for neurite outgrowth in human dorsal root ganglion neurons

doi: 10.1111/ejn.14513

Figure Lengend Snippet: Phospho‐ERK1/2 levels in cultured U2OS‐TrkA/p75‐SHC1 cells and PC12 cells investigated with ELISA. Analysis of pERK1/2 levels in U2OS‐TrkA cells (a) or PC12 cells (b) after NGF stimulation was performed with ELISA. There were significantly increased pERK1/2 levels for NGF‐R100E (*** p = .0005) compared with wild‐type NGF and significantly lower levels for vehicle‐treated U2OS‐TrkA/p75‐SHC1 cells (* p = .0121, a). In b, significantly lower pERK1/2 levels for vehicle‐treated PC12 cells compared with wild‐type NGF were found (* p = .0121). The results are presented as mean ± SEM from four independent biological repeats with one to twelve technical replicates

Article Snippet: Human Phospho‐TrkA DuoSet IC ELISA and Phospho‐ERK1 (T202/Y204)/ERK2 (T185/Y187) DuoSet IC ELISA were from R&D Systems.

Techniques: Cell Culture, Enzyme-linked Immunosorbent Assay