Rabbit Recombinant Monoclonal PCNA antibody. Suitable for IHC-P, ICC, WB and reacts with Human samples. Immunogen corresponding to Synthetic Peptide within Human PCNA aa 200 to C-terminus.
IgG
Rabbit
pH: 8.2
Preservative: 0.09% Sodium azide
Constituents: 99% Borate buffered saline
Liquid
Monoclonal
IHC-P | ICC | WB | |
---|---|---|---|
Human | Tested | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
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Auxiliary protein of DNA polymerase delta and is involved in the control of eukaryotic DNA replication by increasing the polymerase's processibility during elongation of the leading strand. Induces a robust stimulatory effect on the 3'-5' exonuclease and 3'-phosphodiesterase, but not apurinic-apyrimidinic (AP) endonuclease, APEX2 activities. Has to be loaded onto DNA in order to be able to stimulate APEX2. Plays a key role in DNA damage response (DDR) by being conveniently positioned at the replication fork to coordinate DNA replication with DNA repair and DNA damage tolerance pathways (PubMed:24939902). Acts as a loading platform to recruit DDR proteins that allow completion of DNA replication after DNA damage and promote postreplication repair: Monoubiquitinated PCNA leads to recruitment of translesion (TLS) polymerases, while 'Lys-63'-linked polyubiquitination of PCNA is involved in error-free pathway and employs recombination mechanisms to synthesize across the lesion (PubMed:24695737).
Proliferating cell nuclear antigen, PCNA, Cyclin, PCNA
Rabbit Recombinant Monoclonal PCNA antibody. Suitable for IHC-P, ICC, WB and reacts with Human samples. Immunogen corresponding to Synthetic Peptide within Human PCNA aa 200 to C-terminus.
Proliferating cell nuclear antigen, PCNA, Cyclin, PCNA
IgG
Rabbit
pH: 8.2
Preservative: 0.09% Sodium azide
Constituents: 99% Borate buffered saline
Liquid
Monoclonal
BLR075G
Affinity purification
Purified from TCS.
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
ab272076 is the BSA-free version of Anti-PCNA antibody [BLR075G] ab265609.
This product is sold under License from Bethyl Laboratories, Inc.
PCNA or Proliferating Cell Nuclear Antigen functions as a sliding clamp for DNA polymerases during DNA replication. This important role enables it to coordinate the orderly duplication of the genome by increasing the processivity of DNA polymerase δ. PCNA weighs approximately 29 kDa and forms a homotrimeric ring structure. It is expressed in the nucleus of cells often found abundantly in proliferating cells. Aside from its main name some people also refer to it as PC10.
This protein serves a core function in cell cycle regulation and DNA repair. PCNA acts as a scaffold for the assembly of numerous proteins involved in DNA processing forming part of the replication fork complex. It interacts with cyclins and cyclin-dependent kinases (CDKs) linking DNA synthesis to cell cycle progression. Furthermore PCNA partners with proteins involved in DNA mismatch repair base excision repair and nucleotide excision repair.
PCNA is integral in the DNA replication and repair pathways. It closely associates with the p21 protein which regulates the cell cycle by inhibiting cyclin-CDK complexes upon DNA damage. PCNA also plays a part in the ubiquitin-proteasome pathway where its modification by ubiquitin impacts how cells respond to DNA damage. This modification recruits specific proteins for DNA repair highlighting its central role in maintaining genomic stability.
PCNA is linked to cancer and autoimmune diseases. Its overexpression is common in various cancers reflecting its role in cell proliferation and the cell cycle. PCNA antibodies are sometimes found in the serum of patients with systemic lupus erythematosus (SLE) a connection also related to alterations in the p21 protein pathway. The interaction between PCNA and disease-specific proteins emphasizes its importance in both cell proliferation and immune system disorders.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Immunohistochemical analysis of formalin-fixed, paraffin-embedded human prostate carcinoma tissue labeling PCNA with Anti-PCNA antibody [BLR075G] ab265609 at 1/250 dilution. Detection: DAB.
This data was developed using the same antibody clone in a different buffer formulation containing Borate buffered saline, BSA, glycerol and sodium azide (Anti-PCNA antibody [BLR075G] ab265609).
Immunocytochemical analysis of formalin-fixed, paraffin-embedded OVCAR-3 cells labeling PCNA with Anti-PCNA antibody [BLR075G] ab265609 at 1/250 dilution. Detection: DAB.
This data was developed using the same antibody clone in a different buffer formulation containing Borate buffered saline, BSA, glycerol and sodium azide (Anti-PCNA antibody [BLR075G] ab265609).
Detection: Chemiluminescence.
This data was developed using the same antibody clone in a different buffer formulation containing Borate buffered saline, BSA, glycerol and sodium azide (Anti-PCNA antibody [BLR075G] ab265609).
Lysates prepared using NETN lysis buffer.
All lanes: Western blot - Anti-PCNA antibody [BLR075G] - BSA and Azide free (ab272076) at 1/1000 dilution
Lane 1: A549 whole cell lysate at 50 µg
Lane 2: Jurkat whole cell lysate at 50 µg
Lane 3: HEK-293T whole cell lysate at 50 µg
Lane 4: RKO whole cell lysate at 50 µg
Lane 5: K562 whole cell lysate at 50 µg
Lane 6: MCF7 whole cell lysate at 50 µg
Lane 7: HeLa whole cell lysate at 50 µg
Lane 8: U-2 OS whole cell lysate at 50 µg
Lane 9: TCMK whole cell lysate at 50 µg
Lane 10: NIH/3T3 whole cell lysate at 50 µg
All lanes: HRP-conjugated goat anti-rabbit IgG
Predicted band size: 29 kDa
Exposure time: 30s
Immunohistochemical analysis of formalin-fixed, paraffin-embedded human ovarian carcinoma tissue labeling PCNA with Anti-PCNA antibody [BLR075G] ab265609 at 1/250 dilution. Detection: DAB.
This data was developed using the same antibody clone in a different buffer formulation containing Borate buffered saline, BSA, glycerol and sodium azide (Anti-PCNA antibody [BLR075G] ab265609).
This data was developed using the same antibody clone in a different buffer formulation containing Borate buffered saline, BSA, glycerol and sodium azide (Anti-PCNA antibody [BLR075G] ab265609).
Paraffin embedded human breast carcinoma tissue stained for PCNA using Anti-PCNA antibody [BLR075G] ab265609 at 1/500 dilution in immunohistochemical analysis. Secondary antibody used HRP-conjugated goat anti-rabbit IgG. Counterstain: DAPI.
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