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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

4.3
SEK97.20 SEK126.20

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

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Description

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

which synthesize nitric oxide from L-arginine

Mutations in this gene are associated with achromatopsia (rod monochromacy) and color blindness

The encoded protein responds to amino acid deprivation by binding uncharged transfer RNAs

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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