COX4 (8D8) Monoclonal Antibody, ALEXA FLUOR 488
COX4 (8D8) Monoclonal Antibody, ALEXA FLUOR 488 Conjugated
Also known as
Anti-COX4 MAb ALEXA FLUOR 488
Conjugated Primary Antibodies
ALEXA FLUOR® 488
Mouse (Mus musculus)
This is a highly specific antibody against COX4.
1ug per 1ul
Recombinant human COX4 protein
Gene ID Number
Human, Mouse, Rat
Cross-reactive species details
Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.
Background of the antigen
This protein is one of the nuclear-coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport.
Purified by Protein G.
Store this antibody in aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide. Keep refrigerated at 2 to 8 degrees Celcius for up to one year.
Cytochrome c oxidase subunit 4 isoform 1, mitochondrial; COX4I1
For facs or microscopy Alexa 1 conjugate. Alexa Fluor 488 has the same range to that of fluorescein isothiocyanate (FITC), yet the COX4 (8D8) Monoclonal Antibody, has a very high photo stability. As a result of this photo stability, it has turned into an antibody for fluorescent microscopy and FACS FLOW cytometry. It is distinguished in the FL1 of a FACS-Calibur or FACScan. Also Alexa Fluor 488 is pH stable. If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies. ALEXA FLUOR they should be stored frozen at - 24°C for long term storage and for short term at + 5°C.
Monoclonals of this antigen are available in different clones. Each murine monoclonal anibody has his own affinity specific for the clone. Mouse monoclonal antibodies are purified protein A or G and can be conjugated to FITC for flow cytometry or FACS and can be of different isotypes.
COX4 (8D8) Monoclonal Antibody,
Antibody, antibodies against human proteins, antibodies for, Monoclonals or monoclonal antibodies
ALEXA FLUOR 488
COX4 (8D8) monoclonal (Antibody to), ALEXA FLUOR 488
1. Gene info
Scope note:Identification of proteins or peptides that have been electrophoretically separated by blot transferring from the electrophoresis gel to strips of nitrocellulose paper, followed by labeling with antibody probes.
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