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Zebrafish ak2 Antibody (N-term)

Catalog Number: orb1926173

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SizePriceQuantity
50 μl$ 140.00
100 μl$ 240.00
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100 μl Enquire
DispatchUsually dispatched within 5-10 working days
Product Properties
Catalog Numberorb1926173
CategoryAntibodies
DescriptionZebrafish ak2 Antibody (N-term)
ClonalityPolyclonal
Species/HostRabbit
IsotypeRabbit IgG
ConjugationUnconjugated
ReactivityZebrafish
Form/AppearancePurified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
UniProt IDQ1L8L9
MW26616 Da
Tested applicationsFC, IHC-P, WB
Dilution rangeFC - 1:25, IHC-P - 1:100-500, WB - 1:2000
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
NoteFor research use only
Images
Zebrafish ak2 Antibody (N-term)

All lanes: Anti-Zebrafish ak2 Antibody (N-term) at 1:2000 dilution. Lane 1: Zebrafish lysate. Lane 2: ZF4 whole cell lysate. Lane 3: Zebrafish muscle lysate. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 27 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

Zebrafish ak2 Antibody (N-term)

Staining Zebrafish ak2 in zebra fish body tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 3% BSA for 0.5 hour at room temperature; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody (1/25) for 1 hours at 37°C. A undiluted biotinylated goat polyvalent antibody was used as the secondary antibody.

Zebrafish ak2 Antibody (N-term)

Overlay histogram showing ZF4 cells stained (green line). The cells were fixed with 2% paraformaldehyde (10 min) and then permeabilized with 90% methanol for 10 min. The cells were then icubated in 2% bovine serum albumin to block non-specific protein-protein interactions followed by the antibody (1:25 dilution) for 60 min at 37°C. The secondary antibody used was Goat-Anti-Rabbit IgG, DyLight 488 Conjugated Highly Cross-Adsorbed at 1/400 dilution for 40 min at 37°C. Isotype control antibody (blue line) was rabbit IgG (1 μg/1x10^6 cells) used under the same conditions. Acquisition of > 10000 events was performed.

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