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Probable methyltransferase (By similarity).. Additionally we are shipping and many more products for this protein.
METTL23 mutations cause mild nonsyndromic autosomal recessive intellectual disability in two unrelated families, one from Austria, the other from Pakistan.
METTL23, a transcriptional partner of GABPA (show GABPA ELISA Kits), is essential for human cognition
Located immediately downstream of Jmjd6 (show JMJD6 ELISA Kits), with a bi-directionar promoter between the two.
Probable methyltransferase (By similarity).
methyltransferase-like protein 23
, UPF0563 protein