hCLC1-G972 Blocking Peptide
€363.00
In stock
SKU
AC-BP6329c
Background:
The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. The protein encoded by this gene regulates the electric excitability of the skeletal muscle membrane. Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen).
Other Names:
Chloride channel protein 1, ClC-1, Chloride channel protein, skeletal muscle, CLCN1, CLC1
Target/Specificity:
The synthetic peptide sequence is selected from aa 972~988 of HUMAN CLCN1
Gene Name: CLCN1 {ECO:0000303|PubMed:8533761, ECO:0000312|HGNC:HGNC:2019}
Gene ID: 1180
Primary Accession: P35523
Other Accession: P35524; Q64347
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. The protein encoded by this gene regulates the electric excitability of the skeletal muscle membrane. Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen).
Other Names:
Chloride channel protein 1, ClC-1, Chloride channel protein, skeletal muscle, CLCN1, CLC1
Target/Specificity:
The synthetic peptide sequence is selected from aa 972~988 of HUMAN CLCN1
Gene Name: CLCN1 {ECO:0000303|PubMed:8533761, ECO:0000312|HGNC:HGNC:2019}
Gene ID: 1180
Primary Accession: P35523
Other Accession: P35524; Q64347
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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