100 products were found matching "502-0005"!

Cayman's Microcystin ELISA Kit is a competitive assay that can be used for quantification of microcystin in natural water samples. The assay has a range of 27.4-8,000 pg/ml with a mid-point of approximately 660 pg/ml (50% B/B0) and a sensitivity (80% B/B0) of approximately 196 pg/ml.Synonyms: Microcystin EIA Kit....

Mouse IgG was prepared from normal mouse serum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above.  Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Mouse IgG and...

Guinea Pig IgG was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above.  Guinea Pig IgG whole molecule was assayed by immunoelectrophoresis resulted in a single precipitin arc...

Rat IgG was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above.  Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Rat IgG and anti-Rat Serum....

Chicken IgG whole molecule was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed extensive dialysis against the buffer stated above.  Chicken IgG whole molecule assayed by immunoelectrophoresis resulted in a single precipitin...

Myostatin propeptide purity was determined to be greater than 95% as determined by analysis by UV-Spectroscopy at 280nm and by reducing and non-reducing SDS-pAGE. Protein function: Acts specifically as a negative regulator of skeletal muscle growth. [The UniProt Consortium]

This product was prepared from normal serum by delipidation, salt fractionation, ion exchange chromatography followed by papain digestion and extensive dialysis against the buffer stated above.  Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Cat IgG, anti-Cat IgG F(ab')2 and anti-Cat...

Hamster IgG whole molecule was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above.  Hamster IgG whole molecule was assayed by immunoelectrophoresis resulted in a single...

Cells were grown sub-confluent to approximately (2x10^6) cells in Tumor specialized media and then trypsinized. Cells were harvested and cell pellets were flash frozen and stored at -80°C. Non-viable cell pellet was generated from cell line WM1026. WM1026 is a metastatic human melanoma cell line that displays...

Cells were grown sub-confluent to approximately (2x10^6) cells in Tumor specialized media and then trypsinized. Cells were harvested and cell pellets were flash frozen and stored at -80°C. Non-viable cell pellet was generated from cell line WM3702. WM3702 is a metastatic human melanoma cell line that displays...

Cells were grown sub-confluent to approximately (2x10^6) cells in Tumor specialized media and then trypsinized. Cells were harvested and cell pellets were flash frozen and stored at -80°C. Non-viable cell pellet was generated from cell line WM4002. WM4002 is a metastatic human melanoma cell line. This cell line...

Cells were grown sub-confluent to approximately (2x10^6) cells in Tumor specialized media and then trypsinized. Cells were harvested and cell pellets were flash frozen and stored at -80°C. Non-viable cell pellet was generated from cell line WM902B. WM902B is a tumorigenic (VGP) primary melanoma cell line with...