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AB277477

Human OLFM2 ELISA Kit

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Human OLFM2 ELISA Kit is a Sandwich (quantitative) ELISA for the measurement of Human OLFM2 in Human in Biofluids, Cell Culture Media samples.

View Alternative Names

NOE2, OLFM2, Noelin-2, Olfactomedin-2

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ELISA - Human OLFM2 ELISA Kit (AB277477)
  • ELISA

Supplier Data

ELISA - Human OLFM2 ELISA Kit (AB277477)

These standard curves are for demonstration only. A standard curve must be run with each assay.

Key facts

Detection method

Colorimetric

Sample types

Plasma, Cell culture supernatant, Serum

Reacts with

Human

Assay type

Sandwich (quantitative)

Sensitivity

= 0.45 ng/mL

Range

0.41 - 100 ng/mL

Assay Platform

Pre-coated microplate (12 x 8 well strips)

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "sELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

Product details

Human OLFM2 ELISA Kit (ab277477) is an in-vitro enzyme-linked immunosorbent assay for the quantitative measurement of Human OLFM2 in serum, plasma and cell culture supernatants.

This assay employs an antibody specific for Human OLFM2 coated on a 96-well plate. Standards and samples are pipetted into the wells and Human OLFM2 present in a sample is bound to the wells by the immobilized antibody. The wells are washed, and biotinylated anti-Human OLFM2 antibody is added. After washing away unbound biotinylated antibody, HRP-conjugated streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of Human OLFM2 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

Precision

[ { "reproducibilityType": "Inter", "sample": "Overall", "replicates": 0, "mean": null, "standardDeviation": null, "coefficientOfVariability": "< 12" }, { "reproducibilityType": "Intra", "sample": "Overall", "replicates": 0, "mean": null, "standardDeviation": null, "coefficientOfVariability": "< 10" } ]

Recovery

[ { "sample": "Serum", "range": "79 - 124 %", "average": "= 102.1" }, { "sample": "Plasma", "range": "69 - 94 %", "average": "= 79.98" }, { "sample": "Cell culture media", "range": "99 - 141 %", "average": "= 121.4" } ]

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
-20°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Olfactomedin 2 (OLFM2) also known as Noelin 2 is a protein encoded by the OLFM2 gene. It has a mass of approximately 60 kDa. OLFM2 localizes primarily to the extracellular matrix and the cytosol. Expression of this protein occurs in several tissues particularly in the nervous system and ocular tissues where it likely plays a role in the cellular makeup and maintenance.
Biological function summary

OLFM2 is involved in neural development and neuroprotection. It often functions as part of larger protein complexes facilitating cell-cell interactions and signal transduction processes. Additionally the protein influences axon guidance and synaptic organization contributing to the development and integrity of neural networks.

Pathways

OLFM2 integrates into various signaling pathways including the Wnt signaling pathway and the TGF-beta signaling pathway. These pathways regulate important processes like cell proliferation and differentiation. The protein often associates with other components like beta-catenin in the Wnt pathway reflecting its involvement in maintaining cellular homeostasis.

OLFM2 has links to conditions such as glaucoma and retinitis pigmentosa. In these cases OLFM2 interacts with proteins like myocilin which play roles in the pathology of these disorders. The disruption in OLFM2 function or expression can lead to altered cellular and molecular processes contributing to the disease's development and progression.

Product protocols

Target data

Involved in transforming growth factor beta (TGF-beta)-induced smooth muscle differentiation. TGF-beta induces expression and translocation of OLFM2 to the nucleus where it binds to SRF, causing its dissociation from the transcriptional repressor HEY2/HERP1 and facilitating binding of SRF to target genes (PubMed : 25298399). Plays a role in AMPAR complex organization (By similarity). Is a regulator of vascular smooth-muscle cell (SMC) phenotypic switching, that acts by promoting RUNX2 and inhibiting MYOCD binding to SRF. SMC phenotypic switching is the process through which vascular SMCs undergo transition between a quiescent contractile phenotype and a proliferative synthetic phenotype in response to pathological stimuli. SMC phenotypic plasticity is essential for vascular development and remodeling (By similarity).
See full target information OLFM2
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