tion of ABT-491 and the serotonin receptor antagonist
mepyramine [4]. This suggests that combination therapy
may be efficacious in the treatment of allergic rhinitis.
In summary, ABT-491 is a potent
Physiol., 273(5 Pt 2), F768-776
(1997).
5. Schilperoort -Haun, K. R., and Menino, A. R., Jr.,
Factors affecting cellular outgrowth from porcine
inner cell masses in vitro. J. Anim. Sci., 80(10),
2671
conversion of guanosine-
5’–triphosphate (GTP) to cyclic guanosine-3’,5-
monophosphate (cGMP) and pyrophosphate.1,2 sGC is
an obligate hemoprotein enzyme consisting of α and β
subunits of ∼80 kDa and ∼70 kDa respectively
8034-8038.
12 Wingfield, P. et al. (1986) Eur. J. Biochem. 160, 491-497.Wingfield,
P. et al. (1986) Eur. J. Biochem. 160, 491-497.
13 Furutani, Y. et al. (1986) Nucleic Acids Res. 14, 3167-3179.
°C
Synonyms: KRS1; MST2
Product Description
STK3, also known as MST2, encodes a protein of
491 amino acids which contains an N-terminal catalytic
domain characteristic of STKs.1 STK3 and STK4 share
Pierschbacher, M. D. (1987). New perspectives in cell adhesion: RGD
and integrins. Science 238(4826): 491-497.
Important Note: During shipment, small volumes of product will occasionally become entrapped
conversion of
guanosine-5’-triphosphate (GTP) to cyclic
guanosine-3’,5-monophosphate (cGMP) and
pyrophosphate.1,2 sGC is an obligate hemoprotein
enzyme consisting of a and β subunits of ∼80 kDa and
∼70 kDa
conversion of guanosine-
5’-triphosphate (GTP) to cyclic guanosine-3’,5-
monophosphate (cGMP) and pyrophosphate.1,2 sGC is
an obligate hemoprotein enzyme consisting of a and β
subunits of ∼80 kDa and ∼70 kDa
°C
Synonyms: KRS1, MST2
Product Description
STK3, also known as MST2, encodes a protein of
491 amino acids which contains an N-terminal catalytic
domain characteristic of STKs.1 STK3 and STK4 share
0.025, 0.01, 1, 5, or 20 µg/mL, respectively.
Conditioned media was collected at various time points, centrifuged
at 15,000 RPM for 10 min, and the cell-free supernatants were stored
at -80°C prior to assaying
0.025, 0.01, 1, 5, or 20 µg/mL, respectively.
Conditioned media was collected at various time points, centrifuged
at 15,000 RPM for 10 min, and the cell-free supernatants were stored
at -80°C prior to assaying
coassembly of HCN1 and HCN2 subunits
and basal modulation by cyclic nucleotide. J Gen Physiol 117(5), 491-504.
Chen, X., Sirois, J. E., Lei, Q., Talley, E. M., Lynch, C., 3rd, and Bayliss, D. A.
(2005
Primer-directed enzymatic amplification of DNA with a thermostable DNA
polymerase. Science 239 (4839), 487-491 (1988).
Sambrook, J., et al. Molecular Cloning: A Laboratory Manual, third edition, Cold Spring Harbor