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VWA1 Polyclonal Antibody, 50ul Centrifugal Filter Defects in POU4F3 are the
VWA1 Polyclonal Antibody, 50ul Centrifugal Filter Defects in POU4F3 are the
VWA1 Polyclonal Antibody, 50ul Centrifugal Filter Defects in POU4F3 are the
VWA1 Polyclonal Antibody, 50ul Centrifugal Filter Defects in POU4F3 are the

VWA1 Polyclonal Antibody, 50ul Centrifugal Filter Defects in POU4F3 are the

SKU: 2052869687

4.6
PLN162.00 PLN203.00

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VWA1 Polyclonal Antibody, 50ul Centrifugal Filter Defects in POU4F3 are theVWA1 belongs to the von Willebrand factor (VWF; MIM 613160) A (VWFA) domain superfamily of extracellular matrix proteins and appears to play a role in cartilage structure and function (Fitzgerald et al., 2002

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Description

Defects in POU4F3 are the cause of non-syndromic sensorineural deafness autosomal dominant type 15

The CARD domains of both proteins have been shown to specifically interact with BCL10

such as CLASP1

Midline-1 encoded by this MID1 is a member of the tripartite motif (TRIM) family

Mini HCL100 with hot lid to prevent water condensing on the tube cap

VWA1 Polyclonal Antibody, 50ul Centrifugal Filter Defects in POU4F3 are theVWA1 belongs to the von Willebrand factor (VWF; MIM 613160) A (VWFA) domain superfamily of extracellular matrix proteins and appears to play a role in cartilage structure and function (Fitzgerald et al., 2002

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