ODC-1 (Ornithine Decarboxylase-1)(ODC1/486), 0.2mg/mL, Clone: [ODC1/486], Mouse, Monoclonal

Catalog Number: BOT-BNUB0486-500
Article Name: ODC-1 (Ornithine Decarboxylase-1)(ODC1/486), 0.2mg/mL, Clone: [ODC1/486], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNUB0486-500
Supplier Catalog Number: BNUB0486-500
Alternative Catalog Number: BOT-BNUB0486-500-500UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Application: IHC, WB
Species Reactivity: Human, Rat
Immunogen: Recombinant human ODC-1 protein
Alternative Names: Ornithine decarboxylase structural 1, RNODC
Recognizes a 53 kDa protein, identified as the Ornithine Decarboxylase (ODC-1). ODC is the initial and rate-limiting enzyme in the biosynthetic pathway of polyamines and is involved in the conversion of ornithine to putrescine. The biological activity of ODC-1 is rapidly induced in response to virtually all agents known to promote cell proliferation including hormones, drugs, growth factors, mitogens, and tumor promoters. Reportedly, ODC mRNA levels are elevated in lung carcinomas as well as in colon adenomas and carcinomas. ODC activity in colorectal carcinomas is greater than those in adenomas and normal mucosa.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Clonality: Monoclonal
Concentration: 0.2 mg/mL
Clone Designation: [ODC1/486]
Molecular Weight: 53 kDa
UniProt: P11926
Buffer: PBS, 0.05% BSA, 0.05% azide
Source: Animal
Application Notes: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunofluorescence: 0.5-1 ug/mL|Immunohistology formalin-fixed 0.25-0.5 ug/mL|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Western blotting 0.5-1 ug/mL|Optimal dilution for a specific application should be determined by user