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Die folgenden MAPmates™ sollten nicht zusammen analysiert werden: -MAPmates™, die einen unterschiedlichen Assaypuffer erfordern. -Phosphospezifische und MAPmate™ Gesamtkombinationen wie Gesamt-GSK3β und Gesamt-GSK3β (Ser 9). -PanTyr und locusspezifische MAPmates™, z.B. Phospho-EGF-Rezeptor und Phospho-STAT1 (Tyr701). -Mehr als 1 Phospho-MAPmate™ für ein einziges Target (Akt, STAT3). -GAPDH und β-Tubulin können nicht mit Kits oder MAPmates™, die panTyr enthalten, analysiert werden.
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48-602MAG
Buffer Detection Kit for Magnetic Beads
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Anti-PCNA (112-121) (Ab-1) Mouse mAb (PC10): SDB (Sicherheitsdatenblätter), Analysenzertifikate und Qualitätszertifikate, Dossiers, Broschüren und andere verfügbare Dokumente.
Recognizes the ~37 kDa PCNA protein in HeLa cells and in tonsil and normal colon tissue.
Catalogue Number
NA03T
Brand Family
Calbiochem®
Synonyms
Anti-Proliferating Cell Nuclear Antigen
References
References
Waseem, N.H. and Lane, D.P. 1990. J. Cell. Sci.96, 121.
Suzuka, I., et al. 1989. Proc. Natl. Acad. Sci. USA86 3189.
Bravo, R., et al. 1987. Nature (London)326, 515.
Bravo, R. and MacDonald-Bravo, H. 1987. J. Cell. Biol.105, 1549.
Miyachi, K., et al. 1987. J. Immunol.121, 2228.
Product Information
Form
Liquid
Formulation
In 50 mM sodium phosphate buffer, 50% glycerol.
Positive control
HeLa cells, HL-60 cells, tonsil tissue, or normal colon tissue
Preservative
None
Applications
Key Applications
Immunoblotting (Western Blotting)
Immunofluorescence
Not Immunoprecipitation
Paraffin Sections
Application Notes
Immunoblotting (2.5 µg/ml)
Immunofluorescence (1-5 µg/ml)
Immunoprecipitation (not recommended with unconjugated antibody, see comments)
Paraffin Sections (2.5 µg/ml, no pre-treatment required, see comments)
Application Comments
Staining shows an intense nuclear pattern. Not recommended for immunoprecipitation because a ~37 kDa protein will be precipitated that is not PCNA in some samples. Generally, no pre-treatment is needed to stain paraffin sections, but staining may be enhanced in some samples by pre-treating with 4 N HCl for 10 min at 37°C followed by 3 washes in water. Antibody should be titrated for optimal results in individual systems.
Biological Information
Immunogen
recombinant PCNA
Epitope
within amino acids 112-121
Clone
PC10
Host
Mouse
Isotype
IgG2a
Concentration Label
Please refer to vial label for lot-specific concentration
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code
Dry Ice Only
Toxicity
Standard Handling
Storage
-20°C
Protect from Moisture
Protect from moisture
Avoid freeze/thaw
Avoid freeze/thaw
Do not freeze
Ok to freeze
Special Instructions
Following initial thaw, aliquot and freeze (-20°C).
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Bestellnummer
GTIN
NA03T
0
Documentation
Anti-PCNA (112-121) (Ab-1) Mouse mAb (PC10) Analysenzertifikate
Titel
Chargennummer
NA03T
Literatur
Übersicht
Waseem, N.H. and Lane, D.P. 1990. J. Cell. Sci.96, 121.
Suzuka, I., et al. 1989. Proc. Natl. Acad. Sci. USA86 3189.
Bravo, R., et al. 1987. Nature (London)326, 515.
Bravo, R. and MacDonald-Bravo, H. 1987. J. Cell. Biol.105, 1549.
Miyachi, K., et al. 1987. J. Immunol.121, 2228.
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.
Revision
04-September-2007 RFH
Synonyms
Anti-Proliferating Cell Nuclear Antigen
Application
Immunoblotting (2.5 µg/ml)
Immunofluorescence (1-5 µg/ml)
Immunoprecipitation (not recommended with unconjugated antibody, see comments)
Paraffin Sections (2.5 µg/ml, no pre-treatment required, see comments)
Description
Purified mouse monoclonal antibody generated by immunizing BALB/c mice with the specified immunogen and fusing splenocytes with myeloma, SP2/0-Ag14. Recognizes the ~37 kDa PCNA protein.
Background
The proliferating cell nuclear antigen (PCNA) is a ~37 kDa molecular weight protein also known as cyclin. The protein has also been identified as the polymerase δ accessory protein and is detected in a cell cycle dependent manner. In early S phase, PCNA has a very granular distribution and is absent from the nucleoli. At late S phase, PCNA is prominent in the nucleoli. In cells fixed with organic solvents, the PCNA is seen to be strongly associated in the nuclear regions where DNA synthesis is occurring, whereas in cells fixed with aldehydes, the staining is more diffuse but intense and occurs throughout the cell cycle. This is due to the presence of two basic forms of the PCNA protein: a soluble form which is sensitive to organic fixation and not involved in replication and a second form which is insoluble and associated with on-going DNA synthesis. PCNA is a very conserved protein present not only in mammals but also in plant cells. Patients suffering from SLE have been shown to have auto antibodies against PCNA.
Host
Mouse
Immunogen
recombinant PCNA
Epitope
within amino acids 112-121
Clone
PC10
Isotype
IgG2a
Species
human, mouse, rat, yeast
Positive control
HeLa cells, HL-60 cells, tonsil tissue, or normal colon tissue
Form
Liquid
Formulation
In 50 mM sodium phosphate buffer, 50% glycerol.
Concentration Label
Please refer to vial label for lot-specific concentration
Preservative
None
Comments
Staining shows an intense nuclear pattern. Not recommended for immunoprecipitation because a ~37 kDa protein will be precipitated that is not PCNA in some samples. Generally, no pre-treatment is needed to stain paraffin sections, but staining may be enhanced in some samples by pre-treating with 4 N HCl for 10 min at 37°C followed by 3 washes in water. Antibody should be titrated for optimal results in individual systems.
Storage
Protect from moisture
Avoid freeze/thaw
-20°C
Do Not Freeze
Ok to freeze
Special Instructions
Following initial thaw, aliquot and freeze (-20°C).
Toxicity
Standard Handling
References
Waseem, N.H. and Lane, D.P. 1990. J. Cell. Sci.96, 121.
Suzuka, I., et al. 1989. Proc. Natl. Acad. Sci. USA86 3189.
Bravo, R., et al. 1987. Nature (London)326, 515.
Bravo, R. and MacDonald-Bravo, H. 1987. J. Cell. Biol.105, 1549.
Miyachi, K., et al. 1987. J. Immunol.121, 2228.