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Rabbit抗原名称
NF-κB p105/p50分子别名
Nuclear factor NF-kappa-B p105 subunit; DNA-binding factor KBF1; EBP-1; Nuclear factor of kappa light polypeptide gene enhancer in B-cells 1; NFKB1细胞定位
Cytoplasm, NucleusAccession
P19838克隆号
S-3354抗体类型
Recombinant mAb抗体同种型
IgG反应种属 ?
Hu, Ms, Rt阳性样本
HeLa, Jurkat, THP-1, Raji, MCF7, Daudi, A20, mouse spleen, rat spleen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
ChIP
IHC-P ?
WB
稀释度
应用 稀释度 推荐种属 WB 1:1000-1:5000 Hu, Ms, Rt IHC-P 1:500 Hu ChIP 1:20-1:50 Hu
The NF-κB p105 precursor protein is a 105 kDa cytoplasmic ankyrin-repeat-rich molecule that undergoes stimulus-dependent, ubiquitin/proteasome-mediated processing to liberate the 50 kDa DNA-binding p50 subunit, which then dimerizes with other NF-κB/Rel members to form transcriptionally active complexes that rapidly enter the nucleus and regulate genes governing immunity, inflammation, cell survival, and proliferation; p105 itself also serves as an IκB-like inhibitor by sequestering associated dimers in the cytoplasm, and its balanced processing versus full-length stability is tightly controlled by IKK-mediated phosphorylation, ensuring dynamic NF-κB signaling in response to cytokines, pathogens, and cellular stresses.
免疫印迹
WB result of NF-kB p105/p50 Recombinant Rabbit mAb
Primary antibody: NF-kB p105/p50 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: HeLa whole cell lysate 20 µg
Lane 2: Jurkat whole cell lysate 20 µg
Lane 3: THP-1 whole cell lysate 20 µg
Lane 4: Raji whole cell lysate 20 µg
Lane 5: MCF7 whole cell lysate 20 µg
Lane 6: Daudi whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 105 kDa
Observed MW: 50, 105 kDaWB result of NF-kB p105/p50 Recombinant Rabbit mAb
Primary antibody: NF-kB p105/p50 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: A20 whole cell lysate 20 µg
Lane 2: mouse spleen lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 105 kDa
Observed MW: 50, 105 kDaWB result of NF-kB p105/p50 Recombinant Rabbit mAb
Primary antibody: NF-kB p105/p50 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: rat spleen lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 105 kDa
Observed MW: 50, 105 kDa
免疫组化
IHC shows positive staining in paraffin-embedded human tonsil. Anti- NF-kB p105/p50 antibody was used at 1/500 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 gastric cancer. Anti- NF-kB p105/p50 antibody was used at 1/500 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 pancreatic cancer. Anti- NF-kB p105/p50 antibody was used at 1/500 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 lung squamous cell carcinoma. Anti- NF-kB p105/p50 antibody was used at 1/500 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- NF-kB p105/p50 antibody was used at 1/500 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.
ChIP
Chromatin immunoprecipitation (ChIP) was performed on HeLa+hTNF-α (30 ng/ml, 1 hr) cells cross - linked with 1% formaldehyde for 10 min, then chromatin was fragmented by sonication.
Parallel reactions used NF-kB p105/p50 Recombinant Rabbit mAb (S-3354) and Rabbit mAb IgG Isotype Control (SDT-R173) at 1:50 for immunoprecipitation. Post - immunoprecipitation, both samples were washed, eluted, and cross - links reversed. Purified DNA was analyzed by qPCR.
qPCR showed the enrichment of IL-8 and SAT-α in NF-kB p105/p50
Recombinant Rabbit mAb (S-3354)-immunoprecipitated sample.
组织表达图谱
Expression of NF-κB p105/p50 in tumor tissue.
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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