05-479
Anti-Cytochrome C Antibody, clone C-7
ascites fluid, clone C-7, Upstate®
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
Recommended Products
biological source
mouse
antibody form
ascites fluid
antibody product type
primary antibodies
clone
C-7, monoclonal
species reactivity
human, horse
manufacturer/tradename
Upstate®
technique(s)
immunohistochemistry: suitable
western blot: suitable
isotype
IgG
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
human ... CYCS(54205)
Specificity
Cytochrome c
Immunogen
Horse cytochrome c conjugated to KLH
Application
Detect Cytochrome C using this Anti-Cytochrome C Antibody, clone C-7 validated for use in WB, IH.
Research Category
Apoptosis & Cancer
Metabolism
Apoptosis & Cancer
Metabolism
Research Sub Category
Apoptosis - Additional
Enzymes & Biochemistry
Apoptosis - Additional
Enzymes & Biochemistry
Quality
routinely evaluated by immunoblot on RIPA lysates from A431 cells
Target description
14kDa
Linkage
Replaces: 04-1043
Physical form
Ascites
mouse ascites containing 0.05% sodium azide
Storage and Stability
2 years at -20°C
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
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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Product No.
Description
Pricing
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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So-Yeon Kim et al.
Oncotarget, 8(39), 64964-64973 (2016-08-05)
Small molecules to selectively induce cell death of undifferentiated human pluripotent stem cells (hPSCs) have been developed with the aim of lowering the risk of teratoma formation during hPSC-based cell therapy. In this context, we have reported that Quercetin (QC)
Rui Liu et al.
Molecular cancer therapeutics, 14(9), 2090-2102 (2015-07-05)
Tumor adaptive resistance to therapeutic radiation remains a barrier for further improvement of local cancer control. SIRT3, a member of the sirtuin family of NAD(+)-dependent protein deacetylases in mitochondria, promotes metabolic homeostasis through regulation of mitochondrial protein deacetylation and plays
J E Springer et al.
Nature medicine, 5(8), 943-946 (1999-07-30)
Traumatic spinal cord injury often results in complete loss of voluntary motor and sensory function below the site of injury. The long-term neurological deficits after spinal cord trauma may be due in part to widespread apoptosis of neurons and oligodendroglia
Structural basis for the binding of an anti-cytochrome c antibody to its antigen: crystal structures of FabE8-cytochrome c complex to 1.8 A resolution and FabE8 to 2.26 A resolution.
Mylvaganam, S E, et al.
Journal of Molecular Biology, 281, 301-322 (1998)
E A Slee et al.
The Journal of cell biology, 144(2), 281-292 (1999-01-29)
Exit of cytochrome c from mitochondria into the cytosol has been implicated as an important step in apoptosis. In the cytosol, cytochrome c binds to the CED-4 homologue, Apaf-1, thereby triggering Apaf-1-mediated activation of caspase-9. Caspase-9 is thought to propagate
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