| Field | Specification |
|---|---|
| Target | |
| Alternative names | Cytochrome c;CYCS;CYC; |
| UniProt # | |
| Host | |
| Clonality | |
| Isotype | |
| Reactivity | |
| Applications | |
| Immunogen | E.coli-derived human Cytochrome C recombinant protein (Position: G2-E105). Human Cytochrome C shares 91% amino acid (aa) sequence identity with both mouse and rat Cytochrome C. |
| Molecular weight | |
| Purification | |
| Reconstitution | |
| Cellular localization | |
| Concentration | |
| Form | Lyophilized |
| Storage | |
| Catalog no. (Mfr.) | |
| Main SKU |
Product Overview
This rabbit polyclonal antibody targets cytochrome c (gene CYCS) in human, mouse and rat samples and is validated for ICC/IF, IHC and Western blot. The predicted molecular weight is 11.7 kDa, and the supplier reports an observed band at about 14 kDa.
Cytochrome c (CYCS) is a small heme protein in the mitochondrial intermembrane space that shuttles electrons from complex III to complex IV in the respiratory chain. When the outer mitochondrial membrane is permeabilized during apoptosis, it is released into the cytosol, binds APAF1 and triggers the apoptosome and caspase-9 activation, so it is a classic marker of intrinsic apoptosis.
| Target | Cytochrome c (gene CYCS; UniProt P99999, human) |
|---|---|
| Host / Clonality / Isotype | Rabbit / Polyclonal / Rabbit IgG |
| Reactivity | Human, Mouse, Rat |
| Form | Lyophilized |
| Formulation | Per vial: 0.9 mg NaCl; 0.2 mg Na2HPO4; 0.05 mg NaN3; plus stabilizers |
| Calculated MW | 11.7 kDa |
| Observed MW | 14 kDa |
| Storage | As supplied: −20 °C for up to 12 months from receipt. After reconstitution: 4 °C for up to 1 month, or aliquot and keep at −20 °C for up to 6 months. Avoid repeated freeze–thaw cycles. |
Validated Applications
| Western blot | 0.1–0.5 µg/mL (Human, Mouse, Rat) |
|---|---|
| IHC (paraffin sections) | 0.5–1 µg/mL (Human, Mouse, Rat) |
| Immunocytochemistry / Immunofluorescence | 0.5–1 µg/mL (Human) |
| Immunocytochemistry / Immunofluorescence | 2 µg/mL (Human, Mouse, Rat) |
Samples with a confirmed band (WB): human HeLa cells, human 293T cells, human HepG2 cells, rat kidney tissue, rat skeletal muscle tissue, mouse kidney tissue, mouse skeletal muscle tissue.
Recommended loading (WB): 20–40 µg of total protein per lane.
Conditions in the example images (WB): 5–20% gradient SDS-PAGE under reducing conditions, 30 µg lysate per lane, transfer to nitrocellulose membrane, blocking in 5% non-fat milk, primary antibody at 0.5 µg/mL overnight at 4 °C, HRP-conjugated secondary antibody at 1:5000, ECL detection.
Samples with confirmed staining (IHC): mouse brain tissue, rat brain tissue, human intestinal cancer tissue.
Recommended antigen retrieval: heat-mediated, in TE buffer (pH 9.0); citrate buffer (pH 6.0) can be used instead.
Conditions in the example images (IHC): heat-mediated antigen retrieval in citrate buffer (pH 6).
Samples with confirmed staining (ICC/IF): SMMC-7721 cells.
Samples with confirmed staining (ICC/IF): human intestinal cancer tissue, mouse cardiac muscle tissue, rat cardiac muscle tissue.
Immunogen
Recombinant human Cytochrome C fragment (Gly2–Glu105), expressed in E. coli. Sequence identity with the mouse and rat orthologs: 91%.
Reactivity Notes
The supplier lists reactivity with human, mouse and rat. UniProt places cytochrome c in the mitochondrion intermembrane space. The samples tested by the supplier (listed above) are a practical starting point for positive controls.
Safety
Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.
Siyu Chen et al. (2025) Functionalized copper-depleting nanosponges for breast cancer dual starvation favoring dependent energy metabolism and angiogenesis. Chemical Engineering Journal. 10.1016/j.cej.2025.168569
Liangliang Dai et al. (2017) Dual-Targeted Cascade-Responsive Prodrug Micelle System for Tumor Therapy in Vivo. Chemistry of Materials. 10.1021/acs.chemmater.7b02513
Yan Li et al. (2024) Chondroitin sulfate-modified antiangiogenic peptide conjugate induces cell apoptosis via the mitochondria-mediated pathway to perform antitumor activity. International Journal of Biological Macromolecules. 10.1016/j.ijbiomac.2024.129671
Mengchao Ding et al. (2021) A NO/ROS/RNS cascaded-releasing nano-platform for gas/PDT/PTT/immunotherapy of tumors. Biomaterials Science. 10.1039/D1BM00726B
Ling Jin et al. (2022) Circular RNA Rbms1 inhibited the development of myocardial ischemia reperfusion injury by regulating miR-92a/BCL2L11 signaling pathway. Bioengineered. 10.1080/21655979.2022.2025696
Dingchao Zhu et al. (2021) Apigenin enhances viability of random skin flaps by activating autophagy. Phytotherapy Research. 10.1002/ptr.7090
Xie Feng et al. (2021) Anti-Myocardial Ischemia Reperfusion Injury Mechanism of Dried Ginger-Aconite Decoction Based on Network Pharmacology. Frontiers in Pharmacology. 10.3389/fphar.2021.609702
Lu Gan et al. (2015) FABP4 reversed the regulation of leptin on mitochondrial fatty acid oxidation in mice adipocytes. Scientific Reports. 10.1038/srep13588
Ying Wang et al. (2017) Experimental study on the therapeutic effect and underlining mechanisms of positron in pancreatic cancer cells. Oncotarget. 10.18632/oncotarget.18366
Yong He et al. (2014) Inhibitory effects of long noncoding RNA MEG3 on hepatic stellate cells activation and liver fibrogenesis. Biochimica et Biophysica ACTA-Molecular Basis of Disease. 10.1016/j.bbadis.2014.08.015