system, suggesting its involvement in development and
plasticity.8 GAD exists as two isoforms, GAD65 and
GAD67 (molecular masses of 65 and 67 kDa,
respectively) that are encoded by two different
genes
ACID DECARBOXYLASE 65
(GAD 65, 514-530)
Developed in Rabbit, IgG Fraction of Antiserum
Product Number G4913
Product Description
Anti-Glutamic Acid Decarboxylase 65 (GAD 65, 514-
530) is developed
ACID DECARBOXYLASE 65
(GAD 65, 5-22)
Developed in Rabbit, IgG Fraction of Antiserum
Product Number G5038
Product Description
Anti-Glutamic Acid Decarboxylase 65 (GAD 65, 5-22),
is developed
R., et al., Immunol. Lett., 10, 223-252,
(1985)
3. Stevens, R., et al., J. Clin. Immunol., 3, 65-69
(1985).
4. Van der Meulen, F.W., et al., Brit. J. Haematol., 46,
47-56 (1980).
5. Oxelius
(1), 1-8 (1972).
4. Lindqvist, B., et al., Preparative fractionation of
triglyceride mixtures according to acyl carbon
number, using hydroxyalkoxypropyl Sephadex.
J. Lipid Res., 15(1), 65-73 (1974
Hillyard, D.R. et al., A new Conus peptide ligand for
mammalian presynaptic Ca2+ channels. Neuron, 9,
69-77 (1992).
Sold under license from Cognetix for research purposes
only; subject to US patent no
(1), 1−8 (1972).
4. Lindqvist, B., et al., Preparative fractionation of
triglyceride mixtures according to acyl carbon
number, using hydroxyalkoxypropyl Sephadex.
J. Lipid Res., 15(1), 65−73 (1974
., et al., Immunol. Lett., 10, 223 252,
(1985)
3. Stevens, R., et al., J. Clin. Immunol., 3, 65 69
(1985).
4. Van der Meulen, F.W., et al., Brit. J. Haematol.,
46, 47 56 (1980).
at 2-8°C.
REFERENCES: Huff V. Am J Med Genet 1998 Oct 2;79(4):260- 267.
Bruening W, et al. Nat Genet 1992 May;1(2):144-148.
Schedl A, Hastie N. Mol Cell Endocrinol 1998 May 25;140(1-2):65-69.
Monoclonal Anti-phospho-ATF2 (pT69,71) reacts specifi-
cally with ATF2 phosphorylated at both threonine 69
and 71, and does not detect the monophosphorylated
and the non-phosphorylated ATF2 molecule. The
Nail, S. L., et al., Kinetics of acid neutralization by
aluminum hydroxide gel. J. Pharm. Sci., 65(8),
1255-1258 (1976).
7. Geurts, F. L., et al., Encapsulation of aluminium
hydroxide fillers with
, K. F. and Cantley, L. C., Pathways for
phosphoinositide synthesis. Chem. Phys. Lipids,
98(1-2), 69-77 (1999).
3. Vanhaesebroeck, B. and Waterfield, M.D.,
Signaling by distinct classes of phosphoinositide