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Sheep Anti-Mouse IgG ATTO594 (H+L)
Antibody produced in sheep, affinity purified
Cat. #: 3509-1MG
Applications
Suitable as a secondary antibody for immunofluorescence microscopy, flow cytometry, western blotting, and ELISA, depending on assay optimization and detection system.
Description
| Product name |
Sheep Anti-Mouse IgG ATTO594 (H+L) | SXM ATTO594 |
| Target species |
Mouse |
| Description |
Sheep Anti-Mouse IgG ATTO594 (H+L) is an affinity-purified secondary antibody directed against mouse immunoglobulin G, recognizing both heavy and light chains, and is intended for sensitive detection of mouse primary antibodies in standard immunoassays.
ATTO594 has a defined excitation/emission spectrum (λex: 601 nm, λem: 627 nm), supporting red/far-red channel detection in fluorescence-based workflows and multiplex panels, subject to instrument configuration and filter sets.
The antibody is supplied preservative-free to support applications where antimicrobial additives may interfere with downstream procedures (e.g., live-cell or enzyme-sensitive workflows). For best performance, optimize dilution, incubation conditions, and blocking buffer for your specific sample and assay system.
|
| Specification |
Immunofluorescence: 1:500–1:1500, Degree of Labeling (DOL): 2-9, Unconjugated dye ≤5% of total fluorescence. |
| Optical Properties |
λex: 601 nm, λem: 627 nm |
Properties
| Form |
Lyophilized |
| Nominal concentration |
2 mg/ml (after reconstitution with buffer) |
| Content |
1.0 mg Sheep Anti-Mouse IgG ATTO594 (H+L)
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 sheep serum proteins, including immunoglobulins not specifically binding to mouse IgG. After conjugation to the dye, 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 ultrapure reagents in Milli-Q™ water, as described in our publications.
Further Information
Product DataSheet
Material and Safety Data Sheet
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.
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