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RAB3B Antibody

Catalog Number: orb1926122

DispatchUsually dispatched within 5-10 working days
$ 140.00
Catalog Numberorb1926122
CategoryAntibodies
DescriptionPurified Mouse Monoclonal Antibody (Mab)
Species/HostMouse
ClonalityMonoclonal
Clone Number1543CT354.60.92
Tested applicationsFC, IHC-P, WB
ReactivityHuman, Mouse, Rat
IsotypeIgG1,k
Dilution rangeWB: 1:2000, IHC-P: 1:25, FC: 1:25
Form/AppearancePurified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, followed by dialysis against PBS.
ConjugationUnconjugated
MW24758 Da
TargetThis RAB3B antibody is generated from a mouse immunized with a recombinant protein of human RAB3B.
UniProt IDP20337
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
Alternative namesRas-related protein Rab-3B, RAB3B
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NoteFor research use only
Expiration Date12 months from date of receipt.
RAB3B Antibody

All lanes: Anti-RAB3B Antibody at 1:2000 dilution. Lane 1: mouse brain lysate. Lane 2: rat brain lysate. Lane 3: SW480 whole cell lysate. Lane 4: human brain lysate. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-mouse IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 25 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

RAB3B Antibody

Staining RAB3B in human pancreas 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.

RAB3B Antibody

Overlay histogram showing HepG2 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-Mouse IgG, DyLight 488 Conjugated Highly Cross-Adsorbed at 1/400 dilution for 40 min at 37°C. Isotype control antibody (blue line) was mouse IgG (1 μg/1x10^6 cells) used under the same conditions. Acquisition of > 10000 events was performed.

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