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43394

Sigma-Aldrich

Anti-Mouse IgG−Atto 550 antibody produced in goat

1 mg/mL protein

Synonym(s):

Atto 550-Anti-Mouse-IgG antibody produced in goat

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.46

conjugate

Atto 550 conjugate

antibody product type

secondary antibodies

clone

polyclonal

form

liquid

contains

50% glycerol as stabilizer

species reactivity

mouse

concentration

1 mg/mL protein

technique(s)

immunofluorescence: suitable
protein array: 2.8 μg/mL

fluorescence

λex 550 nm; λem 576 nm in PBS

storage temp.

−20°C

target post-translational modification

unmodified

Physical form

Atto 550 goat anti-mouse IgG (whole molecule) is provided in unit sizes of 1 ml as 1 mg/ml solutions in 0.1 M sodium phosphate, 0.1 M NaCl, pH 7.5, containing 5 mM sodium azide as a preservative.

Analysis Note

unconjugated dye ≤5% of total fluorescence

Legal Information

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Smart-aggregation imaging for single molecule localization with SPAD cameras.
Gyongy, I.; et al.
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Iain McWilliam et al.
Methods in molecular biology (Clifton, N.J.), 785, 345-361 (2011-09-09)
A significant proportion of protein microarray researchers would like the arrays they develop to become widely used research, screening, validation or diagnostic devices. For this to be achievable the arrays must be compatible with high-throughput techniques that allow manufacturing scale
Jean Defourny et al.
Proceedings of the National Academy of Sciences of the United States of America, 116(16), 8010-8017 (2019-04-03)
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