Nerve Growth Factor?(NGF) is the archetypal?neurotrophin?of a family of?polypeptides?.It has long occupied a critical role in developmental and adult neurobiology for its many important regulatory functions on the survival, growth and differentiation of nerve cells in the peripheral and central nervous system.NGF selectively binds NTRK1, triggering receptor dimerization, autophosphorylation, and activation of downstream pathways (e.g., MAPK, PI3K-Akt), promoting neuronal survival and differentiation.Thus a functional ELISA assay was conducted to detect the interaction of recombinant rat NGF and recombinant human NTRK1. Briefly, NGF was diluted serially in PBS with 0.01% BSA (pH 7.4). Duplicate samples of 100 μl were then transferred to NTRK1-coated microtiter wells and incubated for 1h at 37℃. Wells were washed with PBST and incubated for 1h with anti-NGF pAb, then aspirated and washed 3 times. After incubation with HRP labelled secondary antibody for 1h at 37℃, wells were aspirated and washed 5 times. With the addition of substrate solution, wells were incubated 15-25 minutes at 37℃. Finally, add 50 μL stop solution to the wells and read at 450/630nm immediately. The binding activity of recombinant rat NGF and recombinant human NTRK1 was shown in Figure 1,and this effect was in a dose dependent manner.

Nerve Growth Factor?(NGF) is the archetypal?neurotrophin?of a family of?polypeptides?.It has long occupied a critical role in developmental and adult neurobiology for its many important regulatory functions on the survival, growth and differentiation of nerve cells in the peripheral and central nervous system.NGF selectively binds NTRK1, triggering receptor dimerization, autophosphorylation, and activation of downstream pathways (e.g., MAPK, PI3K-Akt), promoting neuronal survival and differentiation.Thus a functional ELISA assay was conducted to detect the interaction of recombinant rat NGF and recombinant human NTRK1. Briefly, NGF was diluted serially in PBS with 0.01% BSA (pH 7.4). Duplicate samples of 100 μl were then transferred to NTRK1-coated microtiter wells and incubated for 1h at 37℃. Wells were washed with PBST and incubated for 1h with anti-NGF pAb, then aspirated and washed 3 times. After incubation with HRP labelled secondary antibody for 1h at 37℃, wells were aspirated and washed 5 times. With the addition of substrate solution, wells were incubated 15-25 minutes at 37℃. Finally, add 50 μL stop solution to the wells and read at 450/630nm immediately. The binding activity of recombinant rat NGF and recombinant human NTRK1 was shown in Figure 1,and this effect was in a dose dependent manner.