一般描述
Native IgG from rabbit plasma. IgG is a glycoprotein found in serum and tissue fluids. For use as a negative control in parallel with specific rabbit IgG-type primary antibodies.
警告
Toxicity: Standard Handling (A)
外形
In 10 mM sodium phosphate, 0.85% NaCl, 0.05% NaN₃, pH 7.2.
重悬
Following initial thaw, aliquot and freeze (-20°C). Avoid freeze/thaw cycles.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Gregory J Hogan et al.
PLoS biology, 13(11), e1002307-e1002307 (2015-11-21)
Reprogramming of a gene's expression pattern by acquisition and loss of sequences recognized by specific regulatory RNA binding proteins may be a major mechanism in the evolution of biological regulatory programs. We identified that RNA targets of Puf3 orthologs have
Dasari Vasanthi et al.
Scientific reports, 3, 3011-3011 (2013-10-23)
Anterior-posterior body axis in all bilaterians is determined by the Hox gene clusters that are activated in a spatio-temporal order. This expression pattern of Hox genes is established and maintained by regulatory mechanisms that involve higher order chromatin structure and
Jun Li et al.
Theranostics, 11(12), 5970-5985 (2021-04-27)
Overactivation of N-methyl-D-aspartate receptor (NMDAR) in the spinal cord dorsal horn (SDH) in the setting of injury represents a key mechanism of neuropathic pain. However, directly blocking NMDAR or its downstream signaling, interaction between postsynaptic density-95 (PSD-95) and neuronal nitric
Dasari Vasanthi et al.
Development (Cambridge, England), 137(24), 4239-4247 (2010-11-26)
Hox genes are necessary for proper morphogenesis and organization of various body structures along the anterior-posterior body axis. These genes exist in clusters and their expression pattern follows spatial and temporal co-linearity with respect to their genomic organization. This colinearity
Shama Bhatia et al.
Methods in molecular biology (Clifton, N.J.), 1965, 389-403 (2019-05-10)
Chromatin immunoprecipitation (ChIP) is widely used to measure protein-DNA interactions. This protocol outlines a ChIP method used to identify the association of a protein or protein modification (such as a specific histone modification-methylation, acetylation, etc.) of interest with a specific
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