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Recombinant Cleaved PARP1 p25 Monoclonal Antibody (AN301494L)

Recombinant Cleaved PARP1 p25 Monoclonal Antibody - 1
  • Recombinant Cleaved PARP1 p25 Monoclonal Antibody - 1
  • Recombinant Cleaved PARP1 p25 Monoclonal Antibody - 2
  • Recombinant Cleaved PARP1 p25 Monoclonal Antibody - 3
  • +1
All Size Price Qty
100μL $ 380.00
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50μL $ 249.00
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For research use only.

Verified Samples Verified Samples in WB: HeLa, Raw264.7, Jurkat, 3T3
Verified Samples in IHC: Human breast cancer, Human ovarian cancer
Verified Samples in IF: HeLa
Dilution WB 1:500-1:2000,  IHC 1:200-1:1000,  IF 1:50-1:100
Isotype IgG, κ
Host Rabbit
Reactivity Human,  Mouse
Applications WB,  IHC,  IF
Clonality Monoclonal;Recombinant
Immunogen Recombinant human Cleaved PARP1 p25 fragment
Abbre Cleaved PARP1 p25
Synonyms SCA,  ARTD,  Poly[ADP-ribose] synthase,  Poly ADP ribose polymerase,  poly(ADP-ribose) polymerase,  Poly [ADP-ribose] polymerase,  NAD(+) ADP-ribosyltransferase,  ADP-ribosyltransferase diphtheria toxin-like,  pADPRT,  ADPRT,  ADPRT 1,  ADPRT1,  ARTD1,  PARP,  PARP-1,  PPOL,  pADPRT-1,  PARP1,  Cleaved PARP,  ADP-ribosyltransferase diphtheria toxin-like 1,  APOPAIN,  NAD(+) ADP-ribosyltransferase 1,  Poly [ADP-ribose] polymerase 1,  Poly ADP ribose polymerase 1,  poly(ADP-ribose) polymerase 1,  Poly[ADP-ribose] synthase 1,  SCA1,  ADPRT,  ADPRT 1,  ADPRT1,  ARTD1,  pADPRT-1,  PARP,  PARP-1,  poly(ADP-ribose) polymerase 1,  PPOL
Swissprot
Calculated MW 25 kDa
Observed MW 25 kDa

Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include:

1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein.

2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes.

3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1.

4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids).

5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers.

If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.

Cellular Localization Nucleus
Concentration 1 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A purified
Research Areas Cell Biology,  Epigenetics and Nuclear Signaling,  Metabolism,  Cancer
Clone No. A189
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background Poly-ADP-ribosyltransferase that mediates poly-ADP-ribosylation of proteins and plays a key role in DNA repair. Mainly mediates glutamate and aspartate ADP-ribosylation of target proteins: the ADP-D-ribosyl group of NAD+ is transferred to the acceptor carboxyl group of glutamate and aspartate residues and further ADP-ribosyl groups are transferred to the 2'-position of the terminal adenosine moiety, building up a polymer with an average chain length of 20-30 units.
Other Clones

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Unconjugated

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