catalog number :
MBS727540
products type :
ELISA Kit
products full name :
Mouse Complement 1q ELISA Kit
products short name :
Complement 1q
other names :
complement C1q tumor necrosis factor-related protein 5; Complement C1q tumor necrosis factor-related protein 5; complement C1q tumor necrosis factor-related protein 5; myonectin; C1q TNF-alpha-related protein 5; C1q and tumor necrosis factor related protein 5
other gene names :
C1QTNF5; C1QTNF5; CTRP5; CTRP5; UNQ303/PRO344
uniprot entry name :
C1QT5_HUMAN
storage stability :
Store all reagents at 2-8 degree C.
other info1 :
Assay Type: Competitive
other info2 :
Highest Standards: 500ng/mL. Concentration of Standards: Concentration of Standards: 0,25,50,100,250,500ng/mL
products categories :
Immunology
ncbi acc num :
NP_056460.1
ncbi gb acc num :
NM_015645.4
ncbi mol weight :
25,298 Da
ncbi summary :
This gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late-onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled-related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter. [provided by RefSeq, Jun 2013]
uniprot summary :
C1QTNF5: Defects in C1QTNF5 are a cause of late-onset retinal degeneration (LORD). LORD is an autosomal dominant disorder characterized by onset in the fifth to sixth decade with night blindness and punctate yellow-white deposits in the retinal fundus, progressing to severe central and peripheral degeneration, with choroidal neovascularization and chorioretinal atrophy. Protein type: Secreted, signal peptide; Secreted. Chromosomal Location of Human Ortholog: 11q23.3. Cellular Component: collagen. Disease: Late-onset Retinal Degeneration