catalog number :
MBS034343
products type :
ELISA Kit
products full name :
Human 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]
products gene name :
[C1Q]
other gene names :
[C1QTNF5; C1QTNF5; CTRP5; CTRP5]
uniprot entry name :
C1QT5_HUMAN
specificity :
No significant cross-reactivity or interference between this analyte and analogues is observed.
storage stability :
Store all reagents at 2-8 degree C
other info1 :
Samples: Body fluids, tissue homogenates, secretions or feces samples. Assay Type: Quantitative Sandwich. Detection Range: 25 ug/ml - 800 ug/ml. Sensitivity: 2.0 ug/ml.
other info2 :
Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100].
products description :
Background/Introduction: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! This kit is intended to be used for determination the level of C1Q (hereafter termed "analyte") in undiluted original Human body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances.
ncbi acc num :
NP_001265360.1
ncbi gb acc num :
NM_001278431.1
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; Secreted, signal peptide. Chromosomal Location of Human Ortholog: 11q23.3. Cellular Component: collagen. Disease: Late-onset Retinal Degeneration
size4 :
10x96-Strip-Wells