AB5428P
Anti-Per2 Antibody
Chemicon®, from rabbit
Synonym(s):
Period Circadian Protein 2
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Recommended Products
biological source
rabbit
Quality Level
antibody form
affinity purified immunoglobulin
antibody product type
primary antibodies
clone
polyclonal
purified by
affinity chromatography
species reactivity
mouse
manufacturer/tradename
Chemicon®
technique(s)
ELISA: suitable
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
mouse ... Per2(18627)
Specificity
Recognizes mouse Per 2. The immunogen shows no significant sequence homology with Per 1 or Per 3.
SPECIES REACTIVITIES: The immunogen sequence has 77% homology with rat Per2. No significant homology is seen with human Per 2 (Nagase et al. 1997). Reactivity with other species has not been confirmed.
SPECIES REACTIVITIES: The immunogen sequence has 77% homology with rat Per2. No significant homology is seen with human Per 2 (Nagase et al. 1997). Reactivity with other species has not been confirmed.
Immunogen
A 23 amino acid peptide sequence within the C-teriminus of mouse Per 2 (Albretch et al. 1997; Shearman et al. 1997; Sakamoto et al. 1998).
Application
Detect Per2 using this Anti-Per2 Antibody validated for use in ELISA & WB.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Circadian Rhythm & Sleep
Circadian Rhythm & Sleep
Western blot: 1-10 μg/mL using ECL.
ELISA: 50-100 ng of control peptide per well.
Optimal working dilutions must be determined by the end user.
ELISA: 50-100 ng of control peptide per well.
Optimal working dilutions must be determined by the end user.
Physical form
Affinity purified immunoglobulin. Liquid in PBS containing 0.1% BSA and 0.05% sodium azide.
Storage and Stability
Maintain at -20°C in undiluted aliquots for up to 6 months. Avoid repeated freeze/thaw cycles.
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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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wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Kyle Stokes et al.
Cellular and molecular gastroenterology and hepatology, 4(1), 95-114 (2017-06-09)
The gastrointestinal syndrome is an illness of the intestine caused by high levels of radiation. It is characterized by extensive loss of epithelial tissue integrity, which initiates a regenerative response by intestinal stem and precursor cells. The intestine has 24-hour
Fernando Martin Baidanoff et al.
Biomolecules, 12(7) (2022-07-28)
The molecular circadian clock is based on a transcriptional/translational feedback loop in which the stability and half-life of circadian proteins is of importance. Cysteine residues of proteins are subject to several redox reactions leading to S-thiolation and disulfide bond formation
Xiaoqin Liu et al.
PloS one, 7(11), e50602-e50602 (2012-11-29)
Circadian rhythms in metabolism, physiology, and behavior originate from cell-autonomous circadian clocks located in many organs and structures throughout the body and that share a common molecular mechanism based on the clock genes and their protein products. In the mammalian
Peter Podobed et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 307(2), R121-R137 (2014-05-03)
Circadian rhythms are essential to cardiovascular health and disease. Temporal coordination of cardiac structure and function has focused primarily at the physiological and gene expression levels, but these analyses are invariably incomplete, not the least because proteins underlie many biological
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