Recombinant Cytochrome C Monoclonal Antibody (E-AB-81449) elabscience

$260.00
In stock
SKU
E-AB-81449
SizePrice (USD)
100μL$260.00
50μL$160.00

Product Details

AbbreCytochrome C
SynonymsCYC, Cytochrome C, HCS, Somatic, THC4
SwissprotP99999
ReactivityHuman, Mouse, Rat
HostRabbit
ClonalityRabbit Monoclonal
CloneR09-6H3
IsotypeIgG
ApplicationsWB, IHC-P
ConjugationUnconjugated
Concentration300 μg/mL
Buffer50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.05% stabilizer and 0.05% protective protein.
Purification MethodAffinity Purified
ImmunogenA synthetic peptide of human Cytochrome C
Calculated MW12 kDa
Observed MW14 kDa The actual band is not consistent with the expectation. Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include: 1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein. 2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes. 3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1. 4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids). 5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers. If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.
Research AreasCancer, Cell Biology, Cardiovascular, Metabolism, Signal Transduction
Cellular LocalizationMitochondrion matrix.

Product Description

Background: Cytochrome c is a 12-15 kDa electron transporting protein located in the inner mitochondrial membrane. Upon apoptotic stimulation,cytochrome c can be released from mitochondria into cytoplasm,resulting in caspase-3 activation and apoptosis. Measurement of cytochrome c release from the mitochondria is useful for detection of the onset of apoptosis in cells. In addition,cytochrome c can also leave cells and be detectable in extra-cellular medium of apoptotic cells and serum of cancer patients. The level of serum cytochrome c may serve as a prognostic maker during cancer therapy.

Storage and Shipping

StorageStore at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
ShippingThe product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

Additional Information

Verified SamplesVerified Samples in WB: Jurkat, Rat Rat Brain, C6 Verified Samples in IHC: Human tonsil
DilutionWB 1:1000-1:2000, IHC 1:50-1:100
  1. Phosphocreatine Mitigates Doxorubicin-Induced Neurotoxicity in Rats by Regulating Mitochondrial Function and Apoptosis via the NF-κB/PGC-1α Pathway
    Journal: NEUROMOLECULAR MEDICINE | Year: 2025 | Impact Factor: 3.900
    DOI: 10.1007/s12017-025-08872-y | Reactivity: Rat | Sample Type: brain tissue
  2. Potential anti-liver cancer targets and mechanisms of kaempferitrin based on network pharmacology, molecular docking and experimental verification
    Journal: COMPUTERS IN BIOLOGY AND MEDICINE | Year: 2024 | Impact Factor: 7.000
    DOI: 10.1016/j.compbiomed.2024.108693 | Reactivity: Mouse, Human | Sample Type: SMMC-7721 cell-Xenograft, SMMC-7721 cell
  3. Phosphocreatine attenuates doxorubicin-induced nephrotoxicity through inhibition of apoptosis, and restore mitochondrial function via activation of Nrf2 and PGC-1α pathways
    Journal: CHEMICO-BIOLOGICAL INTERACTIONS | Year: 2024 | Impact Factor: 4.700
    DOI: 10.1016/j.cbi.2024.111147 | Reactivity: Rat | Sample Type: kidney tissue
  4. Quercetin and vitamin E attenuate diabetes-induced testicular anomaly in Wistar rats via the mitochondrial-mediated apoptotic pathway
    Journal: ANDROLOGIA | Year: 2021 | Impact Factor: 2.775
    DOI: 10.1111/and.14185 | Reactivity: Rat | Sample Type: testes

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