HCCS Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP9883c
Background:
The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene.
Other Names:
Cytochrome c-type heme lyase, CCHL, Holocytochrome c-type synthase, HCCS, CCHL
Gene Name: HCCS (HGNC:4837)
Gene ID: 3052
Primary Accession: P53701
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene.
Other Names:
Cytochrome c-type heme lyase, CCHL, Holocytochrome c-type synthase, HCCS, CCHL
Gene Name: HCCS (HGNC:4837)
Gene ID: 3052
Primary Accession: P53701
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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