Rat hippocampus stained with MA1-19352 antibody. Free-floating sections were incubated with MA1-19352 at 1:250 dilution overnight followed by goat anti-mouse conjugated to Cy2 for one hour. Sections were fixed with 4% paraffin. Data courtesy of the Innovators Program.<br />
|Tested species reactivity||Human, Mouse, Pig, Rat|
|Host / Isotype||Mouse / IgM|
|Immunogen||Enriched fraction of porcine brain kinesin.|
|Storage buffer||TBS, pH 8|
|Contains||15mM sodium azide|
|Storage Conditions||4° C, do not freeze|
|Tested Applications||Dilution *|
|Immunocytochemistry (ICC)||Assay Dependent|
|Immunofluorescence (IF)||1:100 - 1:500|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
Kinesin belongs to the group of microtubule-associated motor proteins known to convert chemical energy released from nucleoside triphosphates (preferentially from ATP) into mechanical energy. Conventional kinesin, member of the kinesin superfamily comprising more than 100 proteins, is involved in the anterograde vesicle transport in neuronal cells. Kinesin purified from mammalian brain homogenates is a heterotetramer consisting of two heavy (120 to 130 kDa) and two light chains (60 to 70 kDa), resulting in a molecular mass about 400 kDa. Each heavy chain contains an N-terminal globular motordomain with both a microtubule-binding site and an ATPase active center, stalk region responsible for heavy chain dimerization and finally C-terminal globular tail domain, which is implicated in cargo binding. Light chains may have a regulatory function.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.