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Merck
CN

43394

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

UNSPSC Code:
12352203
NACRES:
NA.46
MDL number:
MFCD06798559

Key Documents

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Product Name

Anti-Mouse IgG−Atto 550 antibody produced in goat, 1 mg/mL protein

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

Quality Level

100

Related Categories

Analysis Note

unconjugated dye ≤5% of total fluorescence

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.

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.

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.

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH8067
BCCM4641
BCCD4079
BCCB9456
BCBS0368V

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Piyush Mishra et al.
Biochemistry and biophysics reports, 11, 138-146 (2017-09-29)
Macroautophagy is a cellular response to starvation wherein superfluous and damaged cytoplasmic constituents are degraded to provide energy for survival and to maintain cellular homeostasis. Dysfunctional autophagy is attributed to disease progression in several pathological conditions and therefore, autophagy has
Juan Eduardo Rodriguez-Gatica et al.
Development (Cambridge, England), 149(20) (2022-07-29)
Organoids are stem cell-derived three-dimensional cultures offering a new avenue to model human development and disease. Brain organoids allow the study of various aspects of human brain development in the finest details in vitro in a tissue-like context. However, spatial
Albino Bacolla et al.
Nucleic acids research, 49(1), 221-243 (2020-12-11)
Human genome stability requires efficient repair of oxidized bases, which is initiated via damage recognition and excision by NEIL1 and other base excision repair (BER) pathway DNA glycosylases (DGs). However, the biological mechanisms underlying detection of damaged bases among the
Baptiste Libé-Philippot et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(30), 7765-7774 (2017-07-15)
Many genetic forms of congenital deafness affect the sound reception antenna of cochlear sensory cells, the hair bundle. The resulting sensory deprivation jeopardizes auditory cortex (AC) maturation. Early prosthetic intervention should revive this process. Nevertheless, this view assumes that no
Jean Defourny et al.
Proceedings of the National Academy of Sciences of the United States of America, 116(16), 8010-8017 (2019-04-03)
Noise overexposure causes oxidative stress, leading to auditory hair cell damage. Adaptive peroxisome proliferation involving pejvakin, a peroxisome-associated protein from the gasdermin family, has been shown to protect against this harmful oxidative stress. However, the role of pejvakin in peroxisome

Articles

Fluorescent Multiplex Detection using Antibody Atto Dye Conjugates

Immunoblotting (Western blot transfer) is a common technique in modern proteomics research.

使用抗体 Atto 染料缀合物进行荧光多重检测

免疫印迹（蛋白质印迹转印）是现代蛋白质组学研究中的常用技术。

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