Human KIF5B peptide (ab41782)
Key features and details
- Purity: > 70% HPLC
- Suitable for: Neutralising, ELISA, Blocking
Description
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Product name
Human KIF5B peptide -
Purity
> 70 % HPLC.
Peptides are analyzed by Reverse-Phase HPLC (RP-HPLC) in order to determine purity. Identities are confirmed by MALDI-MS. -
Accession
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Animal free
No -
Nature
Synthetic -
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Species
Human -
Sequence
CIDEQFDKEKANLEAFTVDKDI -
Amino acids
376 to 396
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Associated products
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Corresponding Antibody
Specifications
Our Abpromise guarantee covers the use of ab41782 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Applications
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Form
Liquid -
Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
General Info
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Alternative names
- Conventional kinesin heavy chain
- KIF 5B
- KIF5B
see all -
Function
Microtubule-dependent motor required for normal distribution of mitochondria and lysosomes. -
Sequence similarities
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. Kinesin subfamily.
Contains 1 kinesin motor domain. -
Domain
Composed of three structural domains: a large globular N-terminal domain which is responsible for the motor activity of kinesin (it hydrolyzes ATP and binds microtubule), a central alpha-helical coiled coil domain that mediates the heavy chain dimerization; and a small globular C-terminal domain which interacts with other proteins (such as the kinesin light chains), vesicles and membranous organelles. -
Cellular localization
Cytoplasm, cytoskeleton. Uniformly distributed between soma and neurites in hippocampal neurons. - Information by UniProt
Protocols
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
Datasheets and documents
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Datasheet download
References (0)
ab41782 has not yet been referenced specifically in any publications.