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Nephrocystin-5 Polyclonal Antibody, 50ul PCR Series Mutations in this gene cause

SKU: 78728641287

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PLN185.00 PLN219.00

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Nephrocystin-5 Polyclonal Antibody, 50ul PCR Series Mutations in this gene causeIQCB1 encodes a nephrocystin protein that interacts with calmodulin and the retinitis pigmentosa GTPase regulator protein. IQ calmodulin binding motif containing protein 1 has a central coiled coil region and two calmodulin binding IQ domains. It is localized to the primary cilia of renal epithelial cells and connecting cilia of photoreceptor cells. IQ calmodulin binding motif containing protein 1 is thought to play a role in ciliary function. Defects

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Description

Mutations in this gene cause cerebellar ataxia in humans

Associates directly or indirectly with lamins at specific cell-cycle stages

Component of the SCF(BTRC) complex containing BTRC

It also plays an important role in trafficking of T cells in thymus

This protein and STAM thus are thought to exhibit compensatory effects on the signaling pathway downstream of JAK kinases upon cytokine stimulation

Nephrocystin-5 Polyclonal Antibody, 50ul PCR Series Mutations in this gene causeIQCB1 encodes a nephrocystin protein that interacts with calmodulin and the retinitis pigmentosa GTPase regulator protein. IQ calmodulin binding motif containing protein 1 has a central coiled coil region and two calmodulin binding IQ domains. It is localized to the primary cilia of renal epithelial cells and connecting cilia of photoreceptor cells. IQ calmodulin binding motif containing protein 1 is thought to play a role in ciliary function. Defects

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