PARP1 Recombinant Rabbit mAb (S-220-179)
Poly [ADP-ribose] polymerase 1,ADP-ribosyltransferase diphtheria toxin-like 1 (ARTD1),DNA ADP-ribosyltransferase PARP1,NAD(+) ADP-ribosyltransferase 1 (ADPRT 1),Poly[ADP-ribose] synthase 1,Protein poly-ADP-ribosyltransferase PARP1,ADPRT,PPOL
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宿主来源
Rabbit分子别名
Poly [ADP-ribose] polymerase 1, ADP-ribosyltransferase diphtheria toxin-like 1 (ARTD1), DNA ADP-ribosyltransferase PARP1, NAD(+) ADP-ribosyltransferase 1 (ADPRT 1), Poly[ADP-ribose] synthase 1, Protein poly-ADP-ribosyltransferase PARP1, ADPRT, PPOL免疫原
Synthetic Peptide细胞定位
Nucleus, CytoplasmAccession
P09874克隆号
S-220-179抗体类型
Recombinant mAb抗体同种型
IgG反应种属 ?
Hu, Ms, Rt预测反应种属
(反应种属缩写表)Bv, Zf, Hm, Av纯化方式
Protein A浓度
0.5 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
储存条件
12 months from date of receipt / reconstitution, -20 °C as supplied
应用
IHC-P ? ,WB稀释度
应用 稀释度 推荐种属 WB 1:1000 Hu IHC-P 1:250 Hu, Ms, Rt
PARP1, short for poly (ADP-ribose) polymerase 1, is an enzyme that plays a pivotal role in DNA repair, maintenance of genomic integrity, and regulation of various metabolic and signaling processes. Discovered over 50 years ago, PARP1 has gradually been recognized for its critical functions in cellular biology. PARP1 catalyzes the transfer of ADP-ribose residues from NAD+ to target substrates, resulting in the formation of a poly (ADP-ribose) (PAR) chain. This PAR modification, known as PARylation, facilitates PARP1's involvement in DNA repair, stabilization of DNA replication forks, and modulation of chromatin structure. The primary functions of PARP1 can be described in four aspects: DNA base excision repair (BER), suppression of transcription from damaged DNA, depletion of cellular energy leading to apoptosis, and participation in transcriptional regulation of certain genes. The loss of PARP1 function has been associated with increased risk of cancers such as breast and lung cancer.
免疫印迹
WB result of PARP1 Rabbit mAb
Primary antibody: PARP1 Rabbit mAb at 1/1000 dilution
Lane 1: untreated HeLa whole cell lysate 20 µg
Lane 2: HeLa treated with 1 μM Staurosporine for 3 hours whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 113 kDa
Observed MW: 120 kDa
免疫组化
IHC shows positive staining in paraffin-embedded human testis. Anti-PARP1 antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human tonsil. Anti-PARP1 antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human cervical squamous cell carcinoma. Anti-PARP1 antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human ovarian carcinoma. Anti-PARP1 antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded mouse testis. Anti-PARP1 mouse testis antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded rat testis. Anti-PARP1 antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
FAQs
我们一般不推荐客户回收利用抗体。 因为抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。另外,我们对一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定

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