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HBB Antibody (C-term)

Catalog Number: orb1938112

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SizePriceQuantity
50 μl$ 140.00
100 μl$ 240.00
50 μl Enquire
100 μl Enquire
DispatchUsually dispatched within 5-10 working days
Product Properties
Catalog Numberorb1938112
CategoryAntibodies
DescriptionHBB Antibody (C-term)
ClonalityPolyclonal
Species/HostRabbit
IsotypeRabbit IgG
ConjugationUnconjugated
ReactivityHuman, Mouse, Rat
Predicted ReactivityBovine, Gallus, Porcine, Rabbit
Form/AppearancePurified polyclonal antibody supplied in PBS with 0.05% (V/V) Proclin 300. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
UniProt IDP68871
MW15998 Da
Tested applicationsFC, IHC-P, WB
Dilution rangeWB - 1:1000
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
Research AreaCardiovascular Research
NoteFor research use only
Expiration Date12 months from date of receipt.
Images
HBB Antibody (C-term)

All lanes: Anti-HBB Antibody (C-term) at 1:2000 dilution. Lane 1: human heart lysate. Lane 2: human liver lysate. Lane 3: K562 whole cell lysate. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 16 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

HBB Antibody (C-term)

HBB Antibody (C-term) immunohistochemistry analysis in formalin fixed and paraffin embedded human liver tissue followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of HBB Antibody (C-term) for immunohistochemistry. Clinical relevance has not been evaluated.

HBB Antibody (C-term)

HBB Antibody (C-term) flow cytometric analysis of K562 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

HBB Antibody (C-term)

Overlay histogram showing K562 cells (green line). The cells were fixed with 4% 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 Alexa Fluor 488 goat anti-rabbit lgG (H+L) (1583138) at 1/400 dilution for 40 min at 37°C. Isotype control antibody (blue line) was rabbit IgG1 (1 μg/1x10^6 cells) used under the same conditions. Acquisition of > 10000 events was performed.

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