CD19 Rabbit Monoclonal Antibody(ARA784)
WB | 1:2000-1:10000 |
IHC | 1:200-1:400 |
IF/ICC | 1:10-1:50 |
FC | 1:50-1:100 |
IP | 1:50 |
Description | Rabbit Monoclonal Antibody to CD19 |
Antibody Type | Primary antibody |
Predicted MW | 61kDa |
Immunogen | A synthetic peptide corresponding to the C-term of CD19 was used as an immunogen. |
Purification | ProA affinity purified IgG |
Form/Buffer | PBS 59%, Sodium azide 0.01%, Glycerol 40%, BSA 0.59%. |
Alternative Names | B-lymphocyte antigen CD19; B-lymphocyte surface antigen B4; Differentiation antigen CD19; T-cell surface antigen Leu-12; CD19 |
Gene Symbol | CD19 |
Entrez Gene | 930(Human) |
Swissprot | P15391 |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

All lanes: Anti-CD19 antibody at 1:2,000 dilution
Predicted MW: 61 kDa
Observed MW: 95 kDa
Lane 1: Ramos
Lane 2: Daudi
Lane 3: Raji
Lysate at 10 µg per lane
2nd Ab:
GAR HRP(H+L) 1:5,000
Exposure: 10s

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of spleen tissue labelling CD19 with ARA784 at 1:400. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9.0.

Anti-CD19 was immunoprecipitated from 0.4mg of Ramos lysate with ARA784 at 1:50 dilution.
2nd Ab:
GAR HRP for IP 1:1,000
Lane 1: ARA784 IP in Ramos whole cell lysate
Lane 2: Rabbit IgG instead of ARA784 in Ramos whole cell lysate
Lane3: Ramos whole cell lysate, 10 µg(input)
Exposure: 60s

Overlay histogram showing Ramos cells stained with ARA784 (Blue). The cells were fixed with 4% paraformaldehyde for 10 mins. The cells were then incubated in the antibody (ARA784, 1:10 dilution) in 1x PBS/1% BSA for 30 min at room temperature . The secondary antibody used was a Goat Anti-Rabbit Alexa Fluor<sup>®</sup> 488 (IgG H+L) at 1:2,000 dilution for 20 min at room temperature. Unlabelled sample (Red) was used as a control.

ARA784 staining CD19 in Raji cells by IF/ICC (Immunocytochemistry/immunofluorescence). Cells were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100 and blocked with 10% goat serum for half an hour at room temperature. Samples were incubated with primary antibody (1:50) at 4°C. An Alexa Fluor<sup>®</sup> 488-conjugated Goat Anti-Rabbit IgG polyclonal was used as the secondary antibody (1:500). DAPI (blue) was used as the nuclear counter stain.
Control: PBS and secondary antibody, An Alexa Fluor<sup>®</sup> 488-conjugated Goat Anti-Rabbit IgG(1:500).
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