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Human CNTF

Human CNTF Quantikine ELISA Kit Summary

Assay Type

Solid Phase Sandwich ELISA

Format

96-well strip plate

Assay Length

3.5 hours or 4.5 hours

Sample Type & Volume Required Per Well

Cell Culture Supernates (200 uL), Serum (200   uL), EDTA Plasma (200 uL), Heparin Plasma (200 uL), Citrate Plasma (200 uL)

Sensitivity

8 pg/mL

Assay Range

31.2 - 2,000 pg/mL (Cell Culture Supernates,   Serum, EDTA Plasma, Heparin Plasma, Citrate Plasma)

Specificity

Recombinant human CNTF

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

The Quantikine Human CNTF Immunoassay is a 3.5 or 4.5 hour solid phase ELISA designed to measure recombinant human CNTF in cell culture supernates, serum, and plasma. It contains recombinant human CNTF and has been shown to accurately quantitate the recombinant factor.

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: CNTF

Ciliary neurotrophic factor (CNTF) is structurally related to IL-6, IL-11, LIF, CLC, and OSM. CNTF was initially identified as a trophic factor for embryonic chick ciliary parasympathetic neurons in culture. Subsequent studies have demonstrated that CNTF is a survival factor for additional neuronal cell types, including dorsal root ganglion sensory neurons, sympathetic ganglion neurons, embryonic motor neurons, major pelvic ganglion neurons and hippocampal neurons.

Long Name:

Ciliary Neurotrophic Factor

Entrez Gene IDs:

1270 (Human); 25707 (Rat)

Alternate Names:

ciliary neurotrophic factor; CNTF; HCNTF

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.

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

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

3Add 50 μL of Assay Diluent to each well.

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

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

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

7Aspirate and wash 5 times.

8Add 100 μL Substrate Solution to each well.

9Add 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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