Goat Anti-Mouse IgG (H+L) ATTO390
Antibody produced in goat, affinity purified
Cat. #: 2101-1MG
Applications
Suited for microscopy and live-cell techniques, containing no preservatives for compatibility with sensitive applications.
Description
| Product name | Goat Anti-Mouse IgG (H+L) ATTO390 | GXM ATTO390 |
| Target species | Mouse |
| Description |
ATTO-labeled secondary antibodies represent a new generation of fluorescent reagents, characterized by their exceptional fluorescence intensity, superior photostability, and consistent performance across various applications. Goat Anti-Mouse IgG ATTO390 is specifically optimized for high-resolution microscopy, offering remarkable photostability and a high fluorescence quantum yield. These properties enable prolonged imaging sessions with minimal photobleaching, ensuring sharp and reliable signals. ATTO390 exhibits a distinct excitation/emission spectrum (390/479 nm), enabling reliable detection in fluorescence-based applications. While its fluorescence characteristics can support multiplex imaging, careful pairing with fluorophores of non-overlapping spectra is essential to minimize spectral overlap. Its compatibility with UV-excitable systems depends on the excitation source, as ATTO390's excitation peak lies at the edge of the UV range. Its strong fluorescence signal and low autofluorescence background make it highly effective in detecting low-abundance targets and achieving precise spatial resolution, even in dense or complex biological samples. This antibody is preservative-free, making it suitable for live-cell imaging and other sensitive applications requiring minimal interference. Its low non-specific binding and high affinity ensure accurate target detection, while its robust fluorescence properties allow consistent results in advanced techniques such as super-resolution microscopy, flow cytometry, and fluorescence resonance energy transfer (FRET) assays. |
| Specification | Immunofluorescence: 1:500–1:1500, Degree of Labeling (DOL): 2-9, Unconjugated dye ≤5% of total fluorescence. |
| Optical Properties | λex: 390 nm, λem: 479 nm |
Properties
| Form | Lyophilized |
| Nominal concentration | 2 mg/ml (after reconstitution with buffer) The antibody is shipped in unit sizes of 1.0 mg as a lyophilized powder, shipped at room temperature. To reconstitute the antibody before use, a glycerol buffer is included for convenience. This allows to re-freeze the antibody after use at -20°C, to keep the quality and/or to prepare aliquots, which can be stored at -20. |
| Content | 1.0 mg Goat Anti-Mouse IgG (H+L) ATTO390 1.0 ml Glycerol buffer (add 0.5 ml to reconstitute the lyophilized antibody) Buffer: 50% glycerol, 0.01 M sodium phosphate, 0.1 M sodium chloride, pH 7.4 |
| Clonality | Polyclonal |
| Isotype | IgG |
| Purification notes | Affinity purification effectively removed all goat serum proteins, including immunoglobulins not specifically binding to mouse IgG. Following conjugation to ATTO390LS the antibody was further purified by gel filtration, resulting in a highly pure and specific antibody. Hypermol® secondary antibodies are highly specific and purified to remove unbound dye, minimizing background signal. |
| Storage instructions | Store as glycerol stock at -20°C. Avoid repeated freeze/thaw cycles. |
| Shipping conditions | Shipped at ambient temperature. |
| Remarks | For Use in Research only. Not for Use in Human or Veterinary Diagnostical or Therapeutical Applications. |
Buffers and antibodies from Hypermol® are made of the purest reagents in Milli-Q™ water, as described in our publications.
Further Information
References
Super-multiplex vibrational imaging.
Wei L, Chen Z, Shi L, Long R, Anzalone AV, Zhang L, Hu F, Yuste R, Cornish VW, Min W.
Nature. 2017 Apr 27;544(7651):465-470. doi: 10.1038/nature22051.
Physiologic and Nanoscale Distinctions Define Glutamatergic Synapses in Tonic vs Phasic Neurons.
He K, Han Y, Li X, et al.
J Neurosci. 2023;43(25):4598-4611. doi:10.1523/JNEUROSCI.0046-23.2023.
Bitbow Enables Highly Efficient Neuronal Lineage Tracing and Morphology Reconstruction in Single Drosophila Brains.
Li Y, et al.
Front Neural Circuits. 2021;15:732183. doi:10.3389/fncir.2021.732183.
Validated product quality with Satisfaction Guarantee!
