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PAX2 mutations can be responsible for renal hypoplasia, either isolated or associated with various ophthalmologic manifestations ranging from retinal coloboma to microphthalmia. Lesions in the PAX6 gene accounts for most cases of aniridia, a congenital malformation of the eye, chiefly characterized by iris hypoplasia, which can cause blindness.

推荐稀释比 IHC:1/100-1/200

Immunohistochemistry analysis of paraffin-embedded Renal Clear Cell Carcinoma using PAX2 antibody.High-pressure and temperature Tris-EDTA pH 8.0 was used for antigen retrieval.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。