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Human Phospho-HGFR/c-MET

Human Phospho-HGFR/c-MET DuoSet IC ELISA Summary

Assay   Type

Solid   Phase Sandwich ELISA

Format

96-well   strip plate

Assay   Length

4.5   hours

Sample   Type & Volume Required Per Well

Cell   lysates (100 μL)

Sensitivity

3.5   pg/mL

Assay   Range

37.5 -   2,400 pg/mL (Cell Culture Supernates, Serum, EDTA Plasma)

Specificity

Natural   and recombinant  human HGF R / c-MET

 

Cross-reactivity

<   0.5% cross-reactivity observed with available related molecules.< 50% cross-species   reactivity observed with species tested

Interference

No   significant interference observed with available related molecules.

Product Summary

This DuoSet IC ELISA contains the basic components required for the development of sandwich ELISAs to measure tyrosine-phosphorylated human HGF R / c-MET in cell lysates. An immobilized capture antibody specific for HGF R / c-MET binds both phosphorylated and unphosphorylated HGF R / c-MET. After washing away unbound material, a biotinylated detection antibody is used to detect only phosphorylated receptor, utilizing a standard HRP format.

Preparation and Storage

Shipping

The   product is shipped at ambient temperature. Upon receipt, store it immediately   at the temperature recommended below.

Storage

Store   the unopened product at 2 - 8 °C. Do not use past expiration date.

Background: HGFR/c-MET

HGF receptor, a product of the proto-oncogene c-met, is a heterodimeric transmembrane glycoprotein that is a receptor-type tyrosine kinase. c-MET is synthesized as a single-chain precursor (pr170) which undergoes post-translational glycosylation and proteolytic cleavage to give rise to the heterodimeric mature form.

Long   Name:

Hepatocyte   Growth Factor Receptor

Entrez   Gene IDs:

4233   (Human); 17295 (Mouse)

Alternate   Names:

AUTS9;   cMET; c-MET; EC 2.7.10; EC 2.7.10.1; hepatocyte growth factor receptor; HGF   R; HGF receptor; HGF/SF receptor; HGFR; Met (c-Met); met proto-oncogene   (hepatocyte growth factor receptor); met proto-oncogene tyrosine kinase; MET;   oncogene MET; Proto-oncogene c-Met; RCCP2; Scatter factor receptor; SF   receptor; Tyrosine-protein kinase Met

Assay Procedure

Refer to the product datasheet for the complete assay procedure.

Bring all reagents and samples to room temperature before use. It is recommended that all samples, standards, and controls be assayed in duplicate.

1.     Prepare all reagents, standard dilutions, and samples as directed in the product insert.

2.     Remove excess microplate strips from the plate frame, return them to the foil pouch containing the desiccant pack, and reseal.

3.     Add 50 μL of Assay Diluent to each well.

4.     Add 50 μL of Standard, control, or sample to each well. Cover with a plate sealer, and incubate at room temperature for 2 hours.

5.     Aspirate each well and wash, repeating the process 4 times for a total of 5 washes.

6.     Add 100 μL of Conjugate to each well. Cover with a new plate sealer, and incubate at room temperature for 2 hours.

7.     Aspirate and wash 5 times.

8.     Add 100 μL Substrate Solution to each well.

9.     Add 100 μL of Stop Solution to each well. Read at 450 nm within 30 minutes. Set wavelength correction to 540 nm or 570 nm.

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