catalog number :
MBS947887
products type :
Recombinant Protein
products full name :
Recombinant Human Loricrin (LOR)
products short name :
Loricrin (LOR)
products name syn :
Loricrin
other names :
loricrin; Loricrin; loricrin; loricrin
products gene name syn :
LOR; LRN
other gene names :
LOR; LOR; LRN
uniprot entry name :
LORI_HUMAN
host :
E Coli or Yeast or Baculovirus or Mammalian Cell
sequence positions :
1-312
sequence :
MSYQKKQPTP QPPVDCVKTS GGGGGGGGSG GGGCGFFGGG GSGGGSSGSG CGYSGGGGYS GGGCGGGSSG GGGGGGIGGC GGGSGGSVKY SGGGGSSGGG SGCFSSGGGG SGCFSSGGGG SSGGGSGCFS SGGGGSSGGG SGCFSSGGGG FSGQAVQCQS YGGVSSGGSS GGGSGCFSSG GGGGSVCGYS GGGSGCGGGS SGGSGSGYVS SQQVTQTSCA PQPSYGGGSS GGGGSGGSGC FSSGGGGGSS GCGGGSSGIG SGCIISGGGS VCGGGSSGGG GGGSSVGGSG SGKGVPICHQ TQQKQAPTWP SK
form :
Liquid containing glycerol; lyophilization may be available upon request.
storage stability :
Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80 degrees C. Store working aliquots at 4 degrees C for up to one week. Repeated freezing and thawing is not recommended.
other info1 :
Species: Homo sapiens (Human)
products description :
Major keratinocyte cell envelope protein.
ncbi acc num :
NP_000418.2
ncbi gb acc num :
NM_000427.2
ncbi summary :
This gene encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases. [provided by RefSeq, Jul 2008]
uniprot summary :
LOR: Major keratinocyte cell envelope protein. Defects in LOR are a cause of progressive symmetric erythrokeratodermia (PSEK). Erythrokeratodermas are a group of disorders characterized by widespread erythematous plaques, either stationary or migratory, associated with features that include palmoplantar keratoderma. PSEK is characterized by erythematous and hyperkeratotic plaques. Defects in LOR are the cause of Vohwinkel syndrome with ichthyosis (VSI); also known as loricrin keratoderma (LK) or mutilating keratoderma with ichthyosis. VSI is an ichthyotic variant of Vohwinkel syndrome (VS) characterized by progressive symmetric erythrokeratoderma or congenital ichthyosiform erythroderma born as a collodion baby. Common clinical features include hyperkeratosis of the palms and soles with digital constriction. Chromosomal Location of Human Ortholog: 1q21. Cellular Component: nucleoplasm; cytoplasm; cornified envelope. Molecular Function: protein binding, bridging; protein binding; structural constituent of cytoskeleton; structural molecule activity. Biological Process: keratinocyte differentiation; keratinization; peptide cross-linking. Disease: Vohwinkel Syndrome, Variant Form
size2 :
0.05 mg (Baculovirus)
size4 :
0.05 mg (Mammalian-Cell)