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POLY(ADP-RIBOSE) POLYMERASE

ArtNr 20-783-70611
Hersteller GENWAY
Menge 0.1 mg
Kategorie
Typ Antibody
Applikationen WB, IP, IHC, ELISA
Clon A6. 4. 12
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-98DF48
Similar products 20-783-70611
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Genway ID:
GWB-98DF48
Specificity:
POLY(ADP-RIBOSE) POLYMERASENCBI
Gene ID:
142
Specificity:
POLY(ADP-RIBOSE) POLYMERASE
Clone:
A6. 4. 12
Immunogen:
Human PARP
Fusion Partner:
Spleen cells from immunised BALB/c mice were fused with cells of mouse NSO myeloma cell line.
Specificity Note:
This product recognises poly (ADP-ribose) polymerase (PARP) a 116kD nuclear enzyme that has been shown to be cleaved during apoptosis.
Immunohistology:
This product requires antigen retrieval using heat treatment prior to staining of paraffin sections. Sodium citrate buffer pH6. 0 is recommended for this purpose.
Preparation:
Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant.
Preservative Stabilisers:
0. 09%Sodium AzideSuggested
Dilution:
Suggested
Dilution:
Western Blotting - 1/1000 - 1/5000 Summary: This protein is a chromatin-associated enzyme poly(ADP-ribosyl)transferase which modifies various nuclear proteins by poly(ADP-ribosyl)ation. The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation proliferation and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage. In addition this enzyme may be the site of mutation in Fanconi anemia and may participate in the pathophysiology of type I diabetes. Summary: This protein is a chromatin-associated enzyme poly(ADP-ribosyl)transferase which modifies various nuclear proteins by poly(ADP-ribosyl)ation. The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation proliferation and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage. In addition this enzyme may be the site of mutation in Fanconi anemia and may participate in the pathophysiology of type I diabetes. 1. Freire. R. et al. (2001) Cleavage of the Bloom\' s syndrome gene product during apoptosis by caspase-3 results in an impaired interaction with topoisomerase IIIalpha. 2. Krohn. A. et al. (1998) Staurosporine-induced apoptosis of cultured rat hippocampal neurons involves caspase-1-like proteases as upstream initiators and increased production of superoxide as a main downstream effector.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 0.1 mg
Lieferbar: In stock
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