MILLIPLEX® MAP Human Kidney Injury Magnetic Bead Panel 2
Kit Catalog # HKI2MAG-99K
Control Catalog # HKI2-6099-2
Lot # HKI2-107 and HKI2-207
Note: The Quality
least 3 years.
References
1. Kase, H., et al., J. Antibiot., 39, 1059-1065 (1986).
2. Hashimoto, S., J. Cell Biol., 107, 1531-1539
(1988).
3. Koizumi, S., et al., J. Neurosci., 8, 715-721 (1988).
4.
lysis buffer
(106−107 cells/ml).
c. For tissues:
Rinse the tissue at least twice with PBS.
Discard the PBS from rinses. Add cell lysis
buffer (5−20 mg tissue/ml).
2. Incubate the cells
44, 5846-5851
(2005).
2. Lin, L.C., et al., Cytotoxic principles from Ventilago
leiocarpa. J. Nat. Prod., 64, 674-676 (2001).
3. Ueno, Y., Induction of apoptosis by T-2 toxin and
other natural
Chromatogr. A, 957(2), 173-185 (2002).
7. Arii, K., et al., Degradation kinetics of
L-alanyl-L-glutamine and its derivatives in
aqueous solution. Eur. J. Pharm. Sci., 7(2),
107-112 (1999).
compounds inhibit mouse mammary cell growth in
vitro by different cellular pathways. Cancer Lett.,
107(2), 277-284 (1996).
6. Morgan, K. T., et al., Application of cDNA
microarray technology to in vitro
compounds inhibit mouse mammary cell growth in
vitro by different cellular pathways. Cancer Lett.,
107(2), 277-284 (1996).
5. Morgan, K.T. et al., Application of cDNA microarray
technology to in vitro
Cells
a. Pellet up to 107 cells. Discard medium.
b. Add 0.5 ml Lysis Solution containing Proteinase K to
cell pellet & vortex.
c. Transfer lysate to filtration column and spin 2 min.
d. Continue to
Product Number B 2629
Storage Temperature 2-8 °C
Product Description
Molecular Formula: C5H11NO2
Molecular Weight: 117.1
CAS Number: 107-43-7
pKa: 1.83
1
Melting Point: 310 °C (with
4. Add cell lysis buffer (106 – 107 cells/mL).
For cells in suspension
1. Collect the cells into an appropriate centrifuge
conical test tube.
2. Centrifuge for 5 minutes at
against invading viral genomes or as
a method to clear a cell of aberrant transcription products1-2.
Cat. #64-101
siIMPORTER™ Transfection Reagent
8
While the mechanism of successful RNAi-mediated
cells
❑ Pellet up to 107 cells. Discard medium.
❑ Mix 10 µl Proteinase K with 0.5 ml Lysis Solution.
Add to cell pellet & vortex.
❑ Transfer lysate to Filtration Column & spin 2 min.
Discard