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Antibodies

Anti-RPSA Antibody (Clone : RP-01)

Product Sizes
0.1 mg
£581.00
30-2497-0.1MG
About this Product
SKU:
30-2497
Additional Names:
Ribosomal protein SA; CCLBP; MRAP; LR1; LRP/LR;ribosomal protein SA
translate.label.attr.clone:
RP-01
Clonality:
Monoclonal
Extra Details:
Ribosomal protein SA (RPSA) is a multi-functional protein; that is an important component of 40S ribosomal subunit; and binds to lamin. Higher expression of RPSA is characteristic for many carcinomas; and correlates with their invasivity and metastatic potential. It has also been described; that RPSA interacts with amyloid beta peptide during Alzheimer´s disease. Specificity : The mouse monoclonal antibody RP-01 recognizes ribosomal protein SA (RPSA); which is important for formation and stability of 40S ribosomal subunit; and is overexpressed in many carcinomas.
Format:
Purified
Immunogen:
REPRLLVVTDPRADHQP
Isotype:
Mouse IgG2a
Purification:
Purified by protein-A affinity chromatography
Reactivities:
Human, Mouse
Shipping Conditions:
Blue Ice
Storage Conditions:
Store at 2-8[o]C. Do not freeze.
Supplier:
Abeomics
Type:
Antibodies
Figure 2: Separation of MOLT-4 cells stained using anti-RPSA (RP-01) purified antibody (red-filled) from MOLT-4 unstained by primary antibody (GAM APC; black-dashed) in flow cytometry analysis (intracellular staining).
Figure 3: Anti-RPSA Purified (clone RP-01) works in WB application under reducing conditions. Western blotting analysis was performed on urea buffer extracts of Ramos; Raji; HeLa; Jurkat; and Huvec cells mixed with hot reducing SDS-loading buffer. Samples were resolved using 10% SDS-PAGE gel. Nitrocellulose membrane blot was probed with mouse IgG2a monoclonal antibody RP-01 (2 µg/ml); followed by IRDye 800CW Goat-anti-Mouse IgG (green). Multiplex fluorescent Western blot detection was perf
Figure 3: Anti-RPSA Purified (clone RP-01) works in WB application under reducing conditions. Western blotting analysis was performed on urea buffer extracts of Ramos; Raji; HeLa; Jurkat; and Huvec cells mixed with hot reducing SDS-loading buffer. Samples were resolved using 10% SDS-PAGE gel. Nitrocellulose membrane blot was probed with mouse IgG2a monoclonal antibody RP-01 (2 µg/ml); followed by IRDye 800CW Goat-anti-Mouse IgG (green). Multiplex fluorescent Western blot detection was perf