biological source
rat
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
1A6, monoclonal
species reactivity
mouse
technique(s)
immunocytochemistry: suitable, immunofluorescence: suitable, western blot: suitable
isotype
IgG2aκ
NCBI accession no.
UniProt accession no.
target post-translational modification
unmodified
Gene Information
mouse ... Cntn5(244682)
General description
Contactin-5 (UniProt P68500; also known as Neural recognition molecule NB-2) is encoded by the Cntn5 gene (Gene ID 244682) in murine species. Contactin-5 (NB-2) is a glycosylphosphatidylinositol (GPI)-anchored glycoprotein belonging to a subgroup of the immunoglobulin superfamily of proteins known as contactins. Five of the six contactins, Contactin-1, contactin-2/TAG-1, contactin-3/BIG-1, contactin-4/BIG-2, and contactin-5/NB-2 are expressed by DRG neurons. Of these, contactin-1, TAG-1, and BIG-2, are also expressed by motor neurons. NB-2 plays an important role in synapse formation in the developing auditory system in rodents. Expression of NB-2 is seen in the central auditory pathways just before the onset of hearing in rodents and is localized at glutamatergic synapses in the postnatal auditory brainstem. NB-2-knockout mice exhibit abnormal responses to auditory stimuli in both neuronal excitability and behavior, and have delayed auditory brainstem response waves. In addition, NB-2 deficiency in mice causes a significant reduction in the number of synapses and induces apoptosis in a subset of neurons in the auditory brainstem. NB-2 is produced with an N-terminal signal peptide (a.a. 1-23) and a C-terminal propeptide (a.a. 1072-1098) sequence, the removal of which yields the mature GPI-anchored glycoprotein (a.a. 24-1071) with six C2-type Ig-like domains (a.a. 98-659) and four type-III fibronectin domains (a.a. 672-1066).
~130 kDa observed. Target band size appears larger than the calculated molecular weights of 120.7/118.0/115.1 kDa (Prepo-/Pro-/mature NB-2) due to glycosylation.
Immunogen
Human IgG Fc-tagged recombinant mouse NB-2/Cntn5.
Application
Research Sub Category
Developmental Neuroscience
Developmental Neuroscience
Research Category
Neuroscience
Neuroscience
This Anti-NB-2 Antibody, clone 1A6 is validated for use in Western Blotting, Immunocytochemistry, Immunofluorescence for the detection of Cntn5.
Western Blotting Analysis: 2.0 ug/mL from a representative lot detected NB-2 in postnatal P14 and adult mouse brain tissue lysates (Courtesy of Dr. Yasushi Shimoda, PhD, Nagaoka University of Technology, Nagaoka, Japan).
Immunocytochemistry Analysis: A representative lot detected punctate NB-2 immunoreactivity on the dendrites of cultured embryonic E17 mouse hippocampal neurons. A partial overlap of NB-2 immunoreactivity with those of APLP1 and synapsin was seen (Shimoda, Y., et al. (2012). Neurosci. Lett. 510(2):148-153).
Immunofluorescence Analysis: A representative lot detected NB-2 immunoreactivity among parvalbumin-/PV-positive proprioceptive sensory neurons by fluorescent immunohistochemistry staining of postnatal day 6 (p6) mouse dorsal root ganglion (DRG) cryosectoins (Ashrafi, S., et al. (2014). Neuron. 81(1):120-129).
Western Blotting Analysis: A representative lot detected NB-2 in presynaptic preparations from the spinal cords of postnatal p6 to p7 mice (Ashrafi, S., et al. (2014). Neuron. 81(1):120-129).
Western Blotting Analysis: A representative lot detected NB-2 in the synaptosomal fractions from mouse cerebral cortex homogenate (Shimoda, Y., et al. (2012). Neurosci. Lett. 510(2):148-153).
Immunocytochemistry Analysis: A representative lot detected punctate NB-2 immunoreactivity on the dendrites of cultured embryonic E17 mouse hippocampal neurons. A partial overlap of NB-2 immunoreactivity with those of APLP1 and synapsin was seen (Shimoda, Y., et al. (2012). Neurosci. Lett. 510(2):148-153).
Immunofluorescence Analysis: A representative lot detected NB-2 immunoreactivity among parvalbumin-/PV-positive proprioceptive sensory neurons by fluorescent immunohistochemistry staining of postnatal day 6 (p6) mouse dorsal root ganglion (DRG) cryosectoins (Ashrafi, S., et al. (2014). Neuron. 81(1):120-129).
Western Blotting Analysis: A representative lot detected NB-2 in presynaptic preparations from the spinal cords of postnatal p6 to p7 mice (Ashrafi, S., et al. (2014). Neuron. 81(1):120-129).
Western Blotting Analysis: A representative lot detected NB-2 in the synaptosomal fractions from mouse cerebral cortex homogenate (Shimoda, Y., et al. (2012). Neurosci. Lett. 510(2):148-153).
Biochem/physiol Actions
Clone 1A6 detected NB-2 in the synaptosomal, but not mitochondrial, fraction from mouse cerebral cortex homogenate (Shimoda, Y., et al. (2012). Neurosci. Lett. 510(2):148-153).
Physical form
Format: Purified
Protein G purified.
Purified rat monoclonal IgG2aκ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Preparation Note
Stable for 1 year at 2-8°C from date of receipt.
Analysis Note
Identity Confirmation by Isotyping Test.
Isotyping Analysis: The identity of this monoclonal antibody is confirmed by isotyping test to be IgG2a.
Isotyping Analysis: The identity of this monoclonal antibody is confirmed by isotyping test to be IgG2a.
Other Notes
Concentration: Please refer to lot specific datasheet.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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存储类别
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Yi-Rong Peng et al.
Neuron, 95(4), 869-883 (2017-08-07)
The size and shape of dendritic arbors are prime determinants of neuronal connectivity and function. We asked how ON-OFF direction-selective ganglion cells (ooDSGCs) in mouse retina acquire their bistratified dendrites, in which responses to light onset and light offset are segregated
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