Mouse anti-CD21 Antibody DL99466A
Specifications
| 50µl / 100µl |
Background:
Mouse monoclonal antibody to CD21
Alternative names:
C3DR; Complement receptor type 2; Cr2; Complement C3d receptor; Epstein-Barr virus receptor; EBV receptor; CD21
Clonality:
Monoclonal
Species reactivity:
H
Host:
Mouse
Immunogen:
KLH-conjugated synthetic peptide encompassing a sequence within human CD21. The exact sequence is proprietary.
Purification method:
The antibody was purified by immunogen affinity chromatography.
Concentration:
1mg/mL
Buffer:
Mouse IgG1. Liquid in PBS containing 50% glycerol, 0.2% BSA and 0.01% sodium azide.
Applications:
IH
Recommended dilution:
IH (1/100 - 1/300)
Storage:
Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
WB description:
N/A
IHC description:
Immunohistochemical analysis of CD21 staining in human follicular lymphoma formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
IF/ICC description:
Immunohistochemical analysis of CD21 staining in human lymphoma formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
IP description:
Immunohistochemical analysis of CD21 staining in human tonsil formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
FC description:
N/A
ChIP description:
N/A
More info:
Email: info@sobekbio.com
Orders:
Email: orders@sobekbio.com
