Neurofilaments can be defined as the intermediate or 10nm filaments found in specifically in neuronal cells.
In the electron microscope neurofilaments appears as 10nm diameter fibres of indeterminate length which generally have fine wispy protrusions from their sides.
They are found particularly abundantly in axons of large projection neurons.
They probably function to provide structural support for neurons and their synapses and to support the large axon diameters required for rapid conduction of impulses down axons.
They are composed a mixture of subunits which usually include the three neurofilament triplet proteins, known as NF-L, NF-M and NF-H.
Neurofilaments may also include smaller amounts of peripherin, alpha-internexin, nestin and in some cases vimentin.
Antibodies to the various neurofilament subunits are very useful cell type markers since the proteins are among the most abundant of the nervous system, are expressed only in neurons, and are biochemically very stable.
The HGNC name for this protein is NEFH.
Applications:Suitable for use in ELISA (capture), Immunofluorescence and Western Blot.
Other applications not tested.
Recommended Dilution:Immunofluorescence: 1:100,000Western Blot: 1:1,000,000Optimal dilutions to be determined by the researcher.
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：50ul
Host：chicken
Source Antibody：bovine
Grade：Purified
Purity：Purified
Form：Supplied as a liquid.
Specificity：Recognizes bovine and rat NF-H. Binds primarily to the phosphorylated axonal forms of NF-H. As with many antibodies to NF-H, this antibody has some cross-reactivity with phosphorylated NF-M, which has similar phosphorylation sites to NF-H.
Isotype：IgY
Calc Applications Abbrev：E IF WB
Calc Crossreactivity：Bo Rt
Immunogen：Bovine intermediate filaments were prepared from spinal cords by the glycerol polymerization method of Delacourte et al., and the cytoskeletal material was dissolved in 6M urea
