PER2 Polyclonal Antibody
规格: | / 20μL / 60μL / 120μL / 200μL |
价格: | / ¥420 / ¥1010 / ¥1640 / ¥2365 |
货号:E-AB-16700
宿主: Rabbit
反应性: H
应用: IHC
Overview
Synonyms | Circadian clock protein PERIOD 2,FASPS,FASPS1,hPER 2,hPER2,KIAA0347,OTTHUMP00000164476,PER 2,PER2,PER2,Period 2,Period 2 isoform 1,Period circadian clock 2,Period circadian protein 2,Period circadian protein homolog 2,Period homolog 2 (Drosophila),Period homolog 2,Period,Drosophila,homolog of,2,Period2,PER2抗体 |
Swissprot | O15055 |
Source | Rabbit |
Reactivity | Human |
Immunogen | Synthetic peptide of human PER2 |
Application | IHC(Detection kit: E-IR-R213) |
Recommended dilution | IHC,,1:100-1:300 |
Concentration | 0.6mg/mL |
Clonality | Polyclonal |
Properties
Cellular localization | Nucleus. Cytoplasm. Mainly nuclear. Nucleocytoplasmic shuttling is effected by interaction with other circadian core oscillator proteins and/or by phosphorylation. Retention of PER1 in the cytoplasm occurs through PER1-PER2 heterodimer formation or by interaction with CSNK1E and/or phosphorylation which appears to mask the PER nuclear localization signal. Also translocated to the nucleus by CRY1 or CRY2. |
Tissue specificity | Widely expressed. Found in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. High levels in skeletal muscle and pancreas. Low level in lung. |
Isotype | IgG |
Purification | Affinity purification |
Conjugation | Unconjugated |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
Background | This gene is a member of the Period family of genes and is expressed in a circadian pattern in the suprachiasmatic Nucleus, the primary circadian pacemaker in the mammalian brain. Genes in this family encode components of the circadian rhythms of locomotor activity, metabolism, and behavior. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene may increase the risk of getting certain cancers and have been linked to sleep disorders. |