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Read our guarantee »Products:Neuroscience >> Neurology process >> Circadian Rhythm
Anti-Cryptochrome I antibody
Cryptochrome I 抗体 (3件) 一覧
Mouse monoclonal to Cryptochrome I
WB, ICC/IF, IHC-P, Flow Cytmore details
Reacts with
Human
Recombinant full length protein, corresponding to amino acids 1-587 of Human Cryptochrome I
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: None
PBS, pH 7.2
Concentration information loading...
Protein G purified
Monoclonal
IgG1
kappa
Neuroscience >> Sensory System >> Visual system
Neuroscience >> Neurotransmission >> Receptors / Channels >> GPCR >> More GPCR
Neuroscience >> Neurology process >> Circadian Rhythm >> Receptors
Neuroscience >> Neurology process >> Circadian Rhythm
Our Abpromise guarantee covers the use of ab54649 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use a concentration of 1 - 5 µg/ml.Predicted molecular weight: 66 kDa.
ICC/IF: Use a concentration of 10 µg/ml
IHC-P: Use a concentration of 5 µg/ml
Flow Cyt: Use 1µg for 106 cells.
Blue light-dependent regulator of the circadian feedback loop. Inhibits CLOCK
NPAS2-ARNTL E box-mediated transcription. Acts, in conjunction with CRY2, in maintaining period length and circadian rhythmicity. Has no photolyase activity. Capable of translocating circadian clock core proteins such as PER proteins to the nucleus. May inhibit CLOCK
NPAS2-ARNTL transcriptional activity through stabilizing the unphosphorylated form of ARNTL.
Belongs to the DNA photolyase class-1 family.
Contains 1 DNA photolyase domain.
Phosphorylation on Ser-247 by MAPK is important for the inhibition of CLOCK-ARNTL-mediated transcriptional activity. Phosphorylation by CSNK1E requires interaction with PER1 or PER2.
Ubiquitinated by the SCF(FBXL3) and SCF(FBXL21) complex leading to degradation.
Cytoplasm. Nucleus. Translocated to the nucleus through interaction with other Clock proteins such as PER2 or ARNTL.
Target information above from: UniProt accessionQ16526
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunofluorescence - Cryptochrome I antibody (ab54649)

Cryptochrome I antibody (ab54649) used in immunofluorescence at 10ug/ml on HeLa cells.
IHC-P - Cryptochrome I antibody (ab54649)

Cryptochrome I antibody (ab54649) used in immunohistochemistry at 5ug/ml on formalin fixed and paraffin embedded human colon adenocarcinoma tissue.
Western blot - Anti-Cryptochrome I antibody (ab54649)

Predicted band size : 66 kDa
Cryptochrome I antibody (ab54649) at 1ug/lane + HeLa cell lysate at 25ug/lane.
Flow Cytometry-Cryptochrome I antibody(ab54649)

Overlay histogram showing HeLa cells stained with ab54649 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab54649, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde/permeabilized in 0.1% PBS-Tween used under the same conditions.
ab54649 has not yet been referenced specifically in any publications.
Publishing research using ab54649? Please let us know so that we can cite the reference in this datasheet
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Cryptochrome I antibody (ab54649) used in immunofluorescence at 10ug/ml on HeLa cells.

Cryptochrome I antibody (ab54649) used in immunohistochemistry at 5ug/ml on formalin fixed and paraffin embedded human colon adenocarcinoma tissue.

Predicted band size : 66 kDa
Cryptochrome I antibody (ab54649) at 1ug/lane + HeLa cell lysate at 25ug/lane.

Overlay histogram showing HeLa cells stained with ab54649 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab54649, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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