Neurturin / Biotin / Polyclonal
Product Details
Description | To detect hNeurturin by Western Blot analysis this antibody can be used at a concentration of 0.1 - 0.2 μg/ml. Used in conjunction with compatible secondary reagents the detection limit for recombinant hNeurturin is 1.5 - 3.0 ng/lane, under either reducing or non-reducing conditions. To detect hNeurturin by sandwich ELISA (using 100 μl/well antibody solution) a concentration of 0.25 – 1.0 μg/ml of this antibody is required. This biotinylated polyclonal antibody, in conjunction with PeproTech's Polyclonal Anti-Human Neurturin (500-P102) as a capture antibody, allows the detection of at least 0.2 – 0.4 ng/well of recombinant hNeurturin. To detect hNeurturin by direct ELISA (using 100 μl/well antibody solution) a concentration of 0.25 – 1.0 μg/ml of this antibody is required. This biotinylated polyclonal antibody, in conjunction with compatible secondary reagents, allows the detection of at least 0.2 – 0.4 ng/well of recombinant hNeurturin.Produced from sera of rabbits pre-immunized with highly pure (>98%) recombinant hNeurturin (human Neurturin). Anti-Human Neurturin specific antibody was purified by affinity chromatography and then biotinylated. | |
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Conjugate | Biotin | |
Clone | Polyclonal | |
Target Species | Human | |
Applications | ELISA, Capture, WB | |
Supplier | PeproTech | |
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About Neurturin
This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein signals through the RET receptor tyrosine kinase and a GPI-linked coreceptor, and promotes survival of neuronal populations. A neurturin mutation has been described in a family with Hirschsprung Disease. [provided by RefSeq, Aug 2016]
This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein signals through the RET receptor tyrosine kinase and a GPI-linked coreceptor, and promotes survival of neuronal populations. A neurturin mutation has been described in a family with Hirschsprung Disease. [provided by RefSeq, Aug 2016]
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