catalog number :
MBS7237764
products type :
ELISA Kit
products full name :
Rat Neogenin ELISA Kit
products short name :
Neogenin
other names :
neogenin; Neogenin; neogenin; neogenin homolog 1; immunoglobulin superfamily DCC subclass member 2; neogenin 1; Immunoglobulin superfamily DCC subclass member 2
other gene names :
NEO1; NEO1; NGN; IGDCC2; NTN1R2; IGDCC2; NGN
uniprot entry name :
NEO1_HUMAN
specificity :
This assay has high sensitivity and excellent specificity for detection of NEO. No significant cross-reactivity or interference between NEO and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between NEO and all the analogues, therefore, cross reaction may still exist in some cases.
storage stability :
Store all reagents at 2-8 degree C.
other info1 :
Samples: Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate. Assay Type: Competitive. Sensitivity: 0.1 ng/mL.
other info2 :
Intended Uses: This NEO ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat NEO. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
products description :
Principle of the assay: NEO ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-NEO antibody and an NEO-HRP conjugate. The assay sample and buffer are incubated together with NEO-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the NEO concentration since NEO from samples and NEO-HRP conjugate compete for the anti-NEO antibody binding site. Since the number of sites is limited, as more sites are occupied by NEO from the sample, fewer sites are left to bind NEO-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The NEO concentration in each sample is interpolated from this standard curve.
ncbi acc num :
AAC51287.1
ncbi mol weight :
158,827 Da
ncbi pathways :
Axon Guidance Pathway (105688); CDO In Myogenesis Pathway (160998); Cell Adhesion Molecules (CAMs) Pathway (83069); Cell Adhesion Molecules (CAMs) Pathway (480); Developmental Biology Pathway (477129); Myogenesis Pathway (160997); Netrin-1 Signaling Pathway (160999)
ncbi summary :
This gene encodes a cell surface protein that is a member of the immunoglobulin superfamily. The encoded protein consists of four N-terminal immunoglobulin-like domains, six fibronectin type III domains, a transmembrane domain and a C-terminal internal domain that shares homology with the tumor suppressor candidate gene DCC. This protein may be involved in cell growth and differentiation and in cell-cell adhesion. Defects in this gene are associated with cell proliferation in certain cancers. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
uniprot summary :
NEO1: May be involved as a regulatory protein in the transition of undifferentiated proliferating cells to their differentiated state. May also function as a cell adhesion molecule in a broad spectrum of embryonic and adult tissues. Belongs to the immunoglobulin superfamily. DCC family. 3 isoforms of the human protein are produced by alternative splicing. Protein type: Membrane protein, integral; Receptor, misc. Chromosomal Location of Human Ortholog: 15q22.3-q23. Cellular Component: integral to plasma membrane; plasma membrane. Molecular Function: cadherin binding; receptor activity. Biological Process: axon guidance; muscle cell differentiation; iron ion homeostasis; regulation of transcription, DNA-dependent; positive regulation of muscle cell differentiation; cell adhesion; myoblast fusion