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Collagen IV alpha2 (Cleaved-Ser1485) Rabbit Polyclonal Antibody, 20ul Deep Well Plates Von Hippel-Lindau syndrome (VHL) is

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Collagen IV alpha2 (Cleaved-Ser1485) Rabbit Polyclonal Antibody, 20ul Deep Well Plates Von Hippel-Lindau syndrome (VHL) isAlpha chains of type IV collagen have a non collagenous domain (NC1) at their C terminus frequent interruptions of the G X Y repeats in the long central triple helical domain (which may cause flexibility in the triple helix) and a short N terminal triple helical 7S domain. Type IV collagen is the major structural component of glomerular basement membranes (GBM) forming a 'chicken wire' meshwork together with laminins proteoglycans and entactin

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Description

Von Hippel-Lindau syndrome (VHL) is a dominantly inherited familial cancer syndrome predisposing to a variety of malignant and benign tumors

In addition to regulating the size of HDL particles

and regulation of cell proliferation

One of two major clathrin-associated adaptor complexes

Acts as a specific chaperone for CENPA and is required for the incorporation of newly synthesized CENPA molecules into nucleosomes at replicated centromeres

Collagen IV alpha2 (Cleaved-Ser1485) Rabbit Polyclonal Antibody, 20ul Deep Well Plates Von Hippel-Lindau syndrome (VHL) isAlpha chains of type IV collagen have a non collagenous domain (NC1) at their C terminus frequent interruptions of the G X Y repeats in the long central triple helical domain (which may cause flexibility in the triple helix) and a short N terminal triple helical 7S domain. Type IV collagen is the major structural component of glomerular basement membranes (GBM) forming a 'chicken wire' meshwork together with laminins proteoglycans and entactin

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