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KIAA1279 encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. Additionally we are shipping KIAA1279 Proteins (5) and many more products for this protein.
Showing 10 out of 23 products:
Human Polyclonal KIAA1279 Primary Antibody for WB - ABIN525596
Drévillon, Megarbane, Demeer, Matar, Benit, Briand-Suleau, Bodereau, Ghoumid, Nasser, Decrouy, Doco-Fenzy, Rustin, Gaillard, Goossens, Giurgea: KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome. in Human molecular genetics 2013
A report on fetal cases with a homozygous mutation in KBP gene in a consanguineous Pakistani family with isolated polymicrogyria.
KBP-cytoskeleton interactions is involved in neuronal development in Goldberg-Shprintzen syndrome.
KBP is a new binding partner for KIF1Balpha that is a regulator of its transport function and thus represents a new type of kinesin interacting protein.
KIF1-binding protein interacts with KIF3A (show KIF3A Antibodies) in haploid male germ cells, promoting spermatid elongation.
KBP expression is up-regulated during neuronal development in mouse cortical neurons.
This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome.
, KIF1 binding protein
, contrapsin-like protease inhibitor 1
, growth hormone-regulated proteinase inhibitor
, kallikrein-binding protein
, serine (or cysteine) peptidase inhibitor, clade A, member 3K
, serine protease inhibitor 2
, serine protease inhibitor 2b
, serine protease inhibitor A3K
, serpin A3K
, thyroid hormone-regulated protein