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LETM1 Rabbit Polyclonal Antibody, 50ul Peptide Modification thus is thought to be

SKU: 57974443889

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PLN162.00 PLN209.00

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LETM1 Rabbit Polyclonal Antibody, 50ul Peptide Modification thus is thought to beThis gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf Hirschhorn syndrome a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8 15 and 19.

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Description

thus is thought to be involved in organogenesis

CCL7 and CCL13 chemokines

SRY-related HMG-box (SOX) genes encode a family of DNA-binding proteins containing a 79-amino acid HMG (high mobility group) domain that shares at least 50% sequence identity with the DNA-binding HMG box of the SRY protein (MIM 480000)

This protein may also function as a tumor suppressor in some cancers

online information:Proteinase 3 entry

LETM1 Rabbit Polyclonal Antibody, 50ul Peptide Modification thus is thought to beThis gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf Hirschhorn syndrome a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8 15 and 19.

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