MFN2 wt Allele

Human MFN2 wild-type allele is located in the vicinity of 1p36.22 and is approximately 33 kb in length. This allele, which encodes mitofusin-2 protein, plays a role in both GTP hydrolysis and mitochondrial fusion. Mutation of the gene is associated with Charcot-Marie-Tooth disease types 2A2 and 6. (NCI Thesaurus)

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MFN2 Gene

This gene is involved in mitochondrial fusion.

MFHAS1 wt Allele

Human MFHAS1 wild-type allele is located in the vicinity of 8p23.1 and is approximately 107 kb in length. This allele, which encodes…

MFHAS1 Gene

This gene is involved in signal transduction.

MFGE8 wt Allele

Human MFGE8 wild-type allele is located within 15q25 and is approximately 15 kb in length. This allele, which encodes lactadherin, is involved…

MFGE8 Gene

This gene plays a regulatory role in the phagocytosis of apoptotic cells.

Mezlocillin Sodium Monohydrate

The monohydrate and sodium salt form of mezlocillin, a broad-spectrum, semisynthetic ampicillin-derived acylureidopenicillin with antibacterial activity. Mezlocillin binds to and inactivates penicillin-binding…