This antibody also recognizes denatured mouse IgG in western blot and immunohistochemistry for formalin-fixed paraffin embedded tissue.
SAB4600199
Anti-Mouse IgG (H+L), highly cross-adsorbed, CF™ 680 antibody produced in goat
~2 mg/mL, affinity isolated antibody
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50 μL
€98.80
0.125 ML
€179.00
€98.80
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50 μL
€98.80
0.125 ML
€179.00
About This Item
UNSPSC Code:
12352203
NACRES:
NA.46
€98.80
Check Cart for Availability
Recommended Products
biological source
goat
Quality Level
conjugate
CF™ 680 conjugate
antibody form
affinity isolated antibody
antibody product type
secondary antibodies
clone
polyclonal
form
buffered aqueous solution
species reactivity
mouse
concentration
~2 mg/mL
technique(s)
flow cytometry: 1-10 μg/mL
immunocytochemistry: suitable
immunohistochemistry: suitable
indirect immunofluorescence: 1-10 μg/mL
fluorescence
λex 681 nm; λem 698 nm
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Related Categories
Specificity
Binds all mouse IgGs
Immunogen
mouse IgG (H+L)
Features and Benefits
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.
Physical form
Supplied in phosphate buffered saline with 0.05% sodium azide, 50% glycerol and 2 mg/mL bovine serum albumin.
Preparation Note
Protect from light.
Legal Information
This product is distributed by Sigma-Aldrich Co. under the authorization of Biotium, Inc. This product is covered by one or more US patents and corresponding patent claims outside the US patents or pending applications owned or licensed by Biotium, Inc. including without limitation: 12/334,387; 12/607,915; 12/699,778; 12/850,578; 61/454,484. In consideration of the purchase price paid by the buyer, the buyer is hereby granted a limited, non-exclusive, non-transferable license to use only the purchased amount of the product solely for the buyer′s own internal research in a manner consistent with the accompanying product literature. Except as expressly granted herein, the sale of this product does not grant to or convey upon the buyer any license, expressly, by implication or estoppel, under any patent right or other intellectual property right of Biotium, Inc. Buyer shall not resell or transfer this product to any third party, or use the product for any commercial purposes, including without limitation, any diagnostic, therapeutic or prophylactic uses. This product is for research use only. Any other uses, including diagnostic uses, require a separate license from Biotium, Inc. For information on purchasing a license to use this product for purposes other than research, contact Biotium, Inc., 3159 Corporate Place, Hayward, CA 94545, Tel: (510) 265-1027. Fax: (510) 265-1352. Email: [email protected].
CF is a trademark of Biotium, Inc.
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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Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue.
Arjan F Theil et al.
Human molecular genetics, 26(23), 4689-4698 (2017-10-04)
The rare recessive developmental disorder Trichothiodystrophy (TTD) is characterized by brittle hair and nails. Patients also present a variable set of poorly explained additional clinical features, including ichthyosis, impaired intelligence, developmental delay and anemia. About half of TTD patients are
Imke K Mandemaker et al.
Journal of cell science, 133(9) (2020-03-19)
Many chromatin remodeling and modifying proteins are involved in the DNA damage response, where they stimulate repair or induce DNA damage signaling. Interestingly, we identified that downregulation of the histone H1 (H1)-interacting protein SET results in increased resistance to a
Arjan F Theil et al.
EMBO molecular medicine, 15(11), e17973-e17973 (2023-10-06)
The brittle hair syndrome Trichothiodystrophy (TTD) is characterized by variable clinical features, including photosensitivity, ichthyosis, growth retardation, microcephaly, intellectual disability, hypogonadism, and anaemia. TTD-associated mutations typically cause unstable mutant proteins involved in various steps of gene expression, severely reducing steady-state
Low dose ionizing radiation strongly stimulates insertional mutagenesis in a γH2AX dependent manner.
Alex N Zelensky et al.
PLoS genetics, 16(1), e1008550-e1008550 (2020-01-17)
Extrachromosomal DNA can integrate into the genome with no sequence specificity producing an insertional mutation. This process, which is referred to as random integration (RI), requires a double stranded break (DSB) in the genome. Inducing DSBs by various means, including
Magdalena Murawska et al.
Cell reports, 37(5), 109944-109944 (2021-11-04)
Heterochromatin formation requires three distinct steps: nucleation, self-propagation (spreading) along the chromosome, and faithful maintenance after each replication cycle. Impeding any of those steps induces heterochromatin defects and improper gene expression. The essential histone chaperone FACT (facilitates chromatin transcription) has
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Est ce que l'anticorps SAB4600199 Sigma-Aldrich Anti-Mouse IgG (H+L), highly cross-adsorbed, CF™ 680 antibody produced in goat ne reconnait que les anticorps non dénaturés (i.e. comme les trueblot). Merci
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