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48-602MAG
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NA19L
Sigma-AldrichAnti-Replication Protein A (Ab-3) Mouse mAb (RPA34-20)
Recognizes the complexed (phosphorylated) and unphosphorylated subunits of replication protein A in HeLa and U293 cells and colon carcinoma tissue.
Catalogue Number
NA19L
Brand Family
Calbiochem®
Synonyms
Anti-RP-A
Application Data
Detection of human replication protein A by immunocytochemical staining. Sample: HeLa cells fixed with methanol. Primary antibody: Anti-Replication Protein A, Human (Mouse) (Cat. No. NA19L) (1.25 μg/ml). Detection: fluorescence.
References
References
Din, S., et al. 1990. Genes Dev.4, 968. Brill, S.J. and Stillman, B. 1989. Nature342, 92. Stillman, B., 1989. Annu. Rev. Cell. Biol.5, 197. Tsurimoto, T. and Stillman, B. 1989. EMBO J.8, 3883. Wobbe, C.R., et al. 1987. Proc. Natl. Acad. Sci.84, 1834.
Product Information
Form
Lyophilized
Formulation
Lyophilized from 20 mM ammonium bicarbonate solution, 100 µg BSA.
Replication protein A (Ab-3) will react with both the complexed (phosphorylated) form of the protein as well as the free (unphosphorylated) 34 kDa subunit. Replication protein A can be used as a marker for cell division. Antibody should be titrated for optimal results in individual systems.
Biological Information
Immunogen
replication protein A purified from U293 cells
Immunogen
Human
Epitope
within the p34 subunit of replication protein A
Clone
RPA34-20
Host
Mouse
Isotype
IgG2a
Species Reactivity
Human
Mouse
Yeast
Antibody Type
Monoclonal Antibody
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code
Ambient Temperature Only
Toxicity
Standard Handling
Storage
+2°C to +8°C
Do not freeze
Ok to freeze
Special Instructions
We recommend resuspending the lyophilized antibody with sterile phosphate buffered saline (PBS), pH 7.4, or sterile 20 mM Tris-saline (20 mM Tris containing 0.15 M NaCl), pH 7.4, to yield a final concentration of 100 µg/ml; product will be more stable if 0.1% sodium azide is included (do not add azide if antibody is to be used with viable cells). Lyophilized antibody should be resuspended at 4°C with occasional gentle mixing for at least 2 h.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Bestellnummer
GTIN
NA19L
0
Documentation
Anti-Replication Protein A (Ab-3) Mouse mAb (RPA34-20) SDB
Anti-Replication Protein A (Ab-3) Mouse mAb (RPA34-20) Analysenzertifikate
Titel
Chargennummer
NA19L
Literatur
Übersicht
Din, S., et al. 1990. Genes Dev.4, 968. Brill, S.J. and Stillman, B. 1989. Nature342, 92. Stillman, B., 1989. Annu. Rev. Cell. Biol.5, 197. Tsurimoto, T. and Stillman, B. 1989. EMBO J.8, 3883. Wobbe, C.R., et al. 1987. Proc. Natl. Acad. Sci.84, 1834.
Datenblatt
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Detection of human replication protein A by immunocytochemical staining. Sample: HeLa cells fixed with methanol. Primary antibody: Anti-Replication Protein A, Human (Mouse) (Cat. No. NA19L) (1.25 μg/ml). Detection: fluorescence.
Description
Purified mouse monoclonal antibody generated by immunizing BALB/c mice with the specified immunogen and fusing splenocytes with NS1 mouse myeloma cells. Recognizes the complexed (phosphorylated) and the ~34 kDa unphosphorylated subunit of replication protein A.
Background
The replication system of a cell contains several essential components among which are replication factor A (RFA, RPA, or HeLa cell SSB), PCNA, and replication factor C (RFC) as well as several other proteins. RPA, a multi-subunit protein containing a 70 kDa, 34 kDa, and 11 kDa protein, may play a critical regulatory role in replication based on its functioning during both the initiation and elongation stages of DNA replication. The protein is highly conserved, having been identified in a range of species from yeast (Saccharomyces cerevisiae) to humans. The primary function of RPA appears to be as an auxiliary protein for both DNA polymerase α and δ. RPA undergoes a cell cycle dependent phosphorylation, which is restricted to the p34 protein. In addition to existing as part of the multi-subunit structure, p34 has also been identified as being present in a free, unphosphorylated form. Recent data shows that RPA is restricted to the nucleus and is overexpressed in transformed cells as well as in several tumor cells.
Host
Mouse
Immunogen species
Human
Immunogen
replication protein A purified from U293 cells
Epitope
within the p34 subunit of replication protein A
Clone
RPA34-20
Isotype
IgG2a
Species
human, mouse, yeast
Positive control
HeLa or U293 cells or colon carcinoma tissue
Form
Lyophilized
Formulation
Lyophilized from 20 mM ammonium bicarbonate solution, 100 µg BSA.
Preservative
None
Comments
Replication protein A (Ab-3) will react with both the complexed (phosphorylated) form of the protein as well as the free (unphosphorylated) 34 kDa subunit. Replication protein A can be used as a marker for cell division. Antibody should be titrated for optimal results in individual systems.
Storage
+2°C to +8°C
Do Not Freeze
Ok to freeze
Special Instructions
We recommend resuspending the lyophilized antibody with sterile phosphate buffered saline (PBS), pH 7.4, or sterile 20 mM Tris-saline (20 mM Tris containing 0.15 M NaCl), pH 7.4, to yield a final concentration of 100 µg/ml; product will be more stable if 0.1% sodium azide is included (do not add azide if antibody is to be used with viable cells). Lyophilized antibody should be resuspended at 4°C with occasional gentle mixing for at least 2 h.
Toxicity
Standard Handling
References
Din, S., et al. 1990. Genes Dev.4, 968. Brill, S.J. and Stillman, B. 1989. Nature342, 92. Stillman, B., 1989. Annu. Rev. Cell. Biol.5, 197. Tsurimoto, T. and Stillman, B. 1989. EMBO J.8, 3883. Wobbe, C.R., et al. 1987. Proc. Natl. Acad. Sci.84, 1834.