|Calculated MW||73262 Da|
|Other Names||Kinesin-like protein KIF22, Kinesin-like DNA-binding protein, Kinesin-like protein 4, KIF22, KID, KNSL4|
|Target/Specificity||A synthetic peptide corresponding to residues on the N-terminus of KID was used as an immunogen.|
|Format||50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA.|
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||KID Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Kinesin family member that is involved in spindle formation and the movements of chromosomes during mitosis and meiosis. Binds to microtubules and to DNA (By similarity). Plays a role in congression of laterally attached chromosomes in NDC80- depleted cells (PubMed:25743205).|
|Cellular Location||Nucleus. Cytoplasm, cytoskeleton|
|Tissue Location||Expressed in bone, cartilage, joint capsule, ligament, skin, and primary cultured chondrocytes|
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Provided below are standard protocols that you may find useful for product applications.
KID (KNSL4; kinesin-like DNA-binding protein) is a member of the kinesin family that is involved in spindle formation and the movements of chromosomes during mitosis and meiosis (1). KID colocalizes with mitotic chromosomes and is enriched in the kinetochore at anaphase. It might play a role in regulating the chromosomal movement along microtubules during mitosis. The N-terminal region of KID shares greater than 35% sequence homology with the motor domains of other kinesins. The C-terminal domain has limited but significant homology to NOD, a Drosophila protein and member of the kinesin family. KID also contains a putative nuclear localization signal (2). It was demonstrated that SIAH, a human homologue of the Drosophila seven in absentia (Sina), is involved in the degradation of KID via the ubiquitin-proteasome pathway (3).
1. Song J, et al. Genomics 52(3):374-7, 1998
2. Tokai N, et al. EMBO J. 15(3):457-67. 1996
3. Germani A, et al. Oncogene 19(52):5997-6006, 2000
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