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Purified Mouse Anti-Per2
Product Details
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BD Transduction Laboratories™
Rat (QC Testing), Mouse (Tested in Development)
Mouse IgG1
Mouse Per2 aa. 1-112
Western blot (Routinely Tested), Immunofluorescence (Tested During Development)
105 kDa
250 µg/ml
AB_398449
Aqueous buffered solution containing BSA, glycerol, and ≤0.09% sodium azide.
RUO


Preparation And Storage

The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. Store undiluted at -20°C.

Product Notices

  1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  2. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
  4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
611138 Rev. 1
Antibody Details
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52/Per2

Circadian rhythms are behavioral or physiological rhythms with periods of approximately 24 hours. They have been identified in many species from bacteria to humans. In mammals, the circadian regulator is the suprachiasmatic nucleus (SCN) of the anterior hypothalamus. Multiple genes involved in the SCN circadian rhythm have been isolated. The Drosophila period (dper) gene is the most completely characterized mammalian clock gene. In mouse, multiple per genes have been identified and constitute a mammalian period gene family (mper1, mper2, and mper3). These proteins contain a dimerization PAS domain and a cytoplasmic localization domain. SCN expression of mper1 and mper2 overlaps,  but is not synchronous. Although not light-inducible, mper2 transcripts are detected approximately two hours following those of mper1. This suggests that the mper1 gene product, a putative transcription factor, is produced in response to light and promotes the expression of mper2. Although mper1 and mper2 are similar, they are not redundant. Thus, these different circadian regulators may allow integration of a wider range of input signals and interact with different downstream effectors.

611138 Rev. 1
Format Details
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Purified
Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
Purified
611138 Rev.1
Citations & References
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Development References (2)

  1. Albrecht U, Sun ZS, Eichele G, Lee CC. A differential response of two putative mammalian circadian regulators, mper1 and mper2, to light. Cell. 1997; 91(7):1055-1064. (Biology). View Reference
  2. Takumi T, Taguchi K, Miyake S. A light-independent oscillatory gene mPer3 in mouse SCN and OVLT. EMBO J. 1998; 17(16):4753-4759. (Biology). View Reference
611138 Rev. 1

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Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described


Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.