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LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Defects in this gene are
LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Defects in this gene are
LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Defects in this gene are
LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Defects in this gene are

LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Defects in this gene are

SKU: 9433705750

4.6
USD97.20 USD120.20

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LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Defects in this gene are

Store: lifelines-uk.org.uk · Domain: lifelines-uk.org.uk

Description

Defects in this gene are cause of an autosomal recessive cutis laxa syndrome

The gene product is linked to enhancement of second messenger-mediated activation of the dopamine beta-hydroylase

Catalytic activity:Palmitoyl-CoA + protein-cysteine = S-palmitoyl protein + CoA

The protein encoded by this gene is 97% identical to the mouse Wnt6 protein at the amino acid level

LRRT4 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Defects in this gene are

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