DYNC1H1 Antibody

The DYNC1H1 gene encodes a cytoplasmic dynein 1 heavy chain 1 protein that is 4,646 amino acids long at 532 kDA. Dyneines function as molecular motors that contain ATPase activity. Defects in DYNC1H1 cause Charcot-Marie-Tooth Disease type 2O (CMT2O), mental retardation autosomal dominant type 13 (MRD13), as well as spinal muscular atrophy, lower extremity, autosomal dominant (SMALED). DYNC1H1 has also been investigated by researchers in myeloma, neuropathy, ciliary dyskinesia, lateral sclerosis, intellectual disabilities, lissencephaly, schizophrenia, malaria, and neurodegeneration. DYNC1H1 participates in centrosome maturation, adaptive immune system, cytoplasmic microtubules, cell cycle spindle assembly and chromosome separation, as well as phagosome and vasopressin-regulated water reabsorption. DYNC1H1 interacts with genes HIST1H4A, HIST1H4B, HIST1H4C, HIST1H4D, and HIST1H43.

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

We have publications tested in 1 confirmed species: Human.

We have publications tested in 2 applications: ICC/IF, WB.

Showing Publication 1 - 1 of 1.

Publication using NBP1-84254	Applications	Species
Marin Barisic, Paulo Aguiar, Stephan Geley et al. Kinetochore motors drive congression of peripheral polar chromosomes by overcoming random arm-ejection forces. Nature Cell Biology 2014-11-10 [PMID: 25383660] (WB, ICC/IF, Human)	WB, ICC/IF	Human

Array NBP1-84254

• DYNC1H1 Antibodies
• DYNC1H1 ELISA Kits
• DYNC1H1 Protein