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M1IP1 Polyclonal Antibody, 20ul Cell Biology Mutations in CCND2 are associated

SKU: 91281208490

4.6
PLN97.20 PLN144.20

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M1IP1 Polyclonal Antibody, 20ul Cell Biology Mutations in CCND2 are associatedIt is uncertain whether Met 1 or Met 2 is the initiator.,Involved in stabilization of microtubules.,Belongs to the SPOT14 family.,subcellular location: Associated with microtubules.,

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Description

Mutations in CCND2 are associated with megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 (MPPH3)

SYNCRIP encodes a member of the cellular heterogeneous nuclear ribonucleoprotein (hnRNP) family

and contains a cleavable hydrophobic peptide with a GPI-anchor site

Alternative splicing of SLC22A5 results in multiple transcript variants

a severe visual disorder

M1IP1 Polyclonal Antibody, 20ul Cell Biology Mutations in CCND2 are associatedIt is uncertain whether Met 1 or Met 2 is the initiator.,Involved in stabilization of microtubules.,Belongs to the SPOT14 family.,subcellular location: Associated with microtubules.,

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