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Catalog Number | orb371663 |
---|---|
Category | Antibodies |
Description | Anti-CD2/CD2 Antibody |
Clonality | Polyclonal |
Species/Host | Rabbit |
Isotype | Rabbit IgG |
Conjugation | Unconjugated |
Reactivity | Mouse |
Form/Appearance | Lyophilized |
Concentration | Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml. |
Immunogen | E. coli-derived mouse CD2 recombinant protein (Position: R23-S203). Mouse CD2 shares 49.7% and 73.3% amino acid (aa) sequence identity with human and rat CD2, respectively. |
UniProt ID | P08920 |
MW | 58 kDa |
Tested applications | IHC, WB |
Application notes | Immunohistochemistry (Paraffin-embedded Section), 0.5-1μg/ml, Mouse Western blot, 0.1-0.5μg/ml, Mouse. Add 0.2ml of distilled water will yield a concentration of 500ug/ml |
Antibody Type | Primary Antibody |
Storage | Maintain 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 names | T-cell surface antigen CD2; LFA-2; LFA-3 receptor; Read more... |
Note | For research use only |
IHC analysis of CD2 using anti-CD2 antibody. CD2 was detected in a paraffin-embedded section of mouse lymphaden tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 µg/ml rabbit anti-CD2 Antibody overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
Western blot analysis of CD2 using anti-CD2 antibody. Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse cardiac muscle tissue lysates, Lane 2: HEPA whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD2 antigen affinity purified polyclonal antibody at 0.5 µg/mL overnight at 4°C, then washed with TBS-0.1% Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for CD2 at approximately 58 kDa. The expected band size for CD2 is at 38 kDa.