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VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Deficiencies in this protein are

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SEK111.00 SEK150.00

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VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Deficiencies in this protein areThis gene encodes a homeobox protein originally described as a retina specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.

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Description

Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss

Defects in this gene are a cause of Walker-Warburg syndrome (WWS)

This protein plays a role in several cellular processes

This encoded protein contains a GRIP domain which is thought to be used in targeting

VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Deficiencies in this protein areThis gene encodes a homeobox protein originally described as a retina specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.

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