Western blot analysis of extracts from thp 1 cells untreated or treated with tnf α and cycloheximide as well as control extracts from sw620 and a20 cell lines using parp 46d11 rabbit mab.
Parp antibody cell signaling technology.
Cell signaling technology s parp antibody is a rabbit polyclonal antibody.
Applications key ab array antibody array abseq abseq ae affinity electrophoresis.
Western blot analysis of extracts from hela cells untreated or treated with staurosporine 9953 1 μm 3 hr jurkat cells untreated or etoposide treated 25 μm overnight and thp 1 cells untreated or cycloheximide treated chx 10 μg ml overnight followed by treatment with tnf α 8902 20 ng ml 4 hr using cleaved parp asp214 d64e10 xp rabbit mab upper or total parp.
Antibody 9532 parp 46d11 rabbit mab by cell signaling technology.
In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding.
This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5.
Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1.
This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5.
Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1.
This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5.
This protein can be cleaved by many ice like caspases in vitro 2 3 and is one of the main cleavage targets of caspase 3 in vivo 4 5.
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Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1.
The absence of signal in the parp knockout hek293 cells confirms the specificity of the antibody for parp.
An antibody shouldn t be one of the variables in your experiment.
Parp a 116 kda nuclear poly adp ribose polymerase appears to be involved in dna repair in response to environmental stress 1.
In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding.
In human parp the cleavage occurs between asp214 and gly215 which separates the parp amino terminal dna binding.
The parp antibody was generated using ppol poly adp ribose polymerase family member 1 parp 1 and parp1 as the antigen.