ATF-4 Recombinant Rabbit mAb (S-471-111)
cAMP-dependent transcription factor ATF-4,Activating transcription factor 4,Cyclic AMP-responsive element-binding protein 2,cAMP-responsive element-binding protein 2,Tax-responsive enhancer element-binding protein 67,CREB2,TXREB,TaxREB67
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宿主来源
Rabbit抗原名称
ATF-4分子别名
cAMP-dependent transcription factor ATF-4; Activating transcription factor 4; Cyclic AMP-responsive element-binding protein 2; cAMP-responsive element-binding protein 2; Tax-responsive enhancer element-binding protein 67; CREB2; TXREB; TaxREB67免疫原
Recombinant Protein细胞定位
Cytoplasm, Nucleus, Cell membraneAccession
P18848克隆号
S-471-111抗体类型
Recombinant mAb抗体同种型
IgG反应种属 ?
Hu, Ms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
ICC ?
WB
稀释度
应用 稀释度 推荐种属 WB 1:1000 Hu, Ms ICC 1:100 Hu ChIP 1:20-1:50 Hu
ATF-4 is a transcription factor that was originally identified as a widely expressed mammalian DNA binding protein that could bind a tax-responsive enhancer element in the LTR of HTLV-1. It belongs to a family of DNA-binding proteins that includes the AP-1 family of transcription factors, cAMP-response element binding proteins (CREBs) and CREB-like proteins. ATF4 transcription factor is also known to play role in osteoblast differentiation along with RUNX2 and osterix. ATF4 is also involved in the cannabinoid Δ9-tetrahydrocannabinol–induced apoptosis in cancer cells, by the proapoptotic role of the stress protein p8 via its upregulation of the endoplasmic reticulum stress-related genes ATF4, CHOP, and TRB3.
免疫印迹
WB result of ATF-4 Rabbit mAb
Primary antibody: ATF-4 Rabbit mAb at 1/1000 dilution
Lane 1: HeLa whole cell lysate 40 µg
Lane 2: HeLa treated with Tunicamycin (2µg/mL, 8hr) whole cell lysate 40 µg
Lane 3: HEK-293 whole cell lysate 40 µg
Lane 4: HEK-293 treated with Tunicamycin (2µg/mL, 8hr) whole cell lysate 40 µg
Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 38 kDa
Observed MW: 50 kDaWB result of ATF-4 Rabbit mAb
Primary antibody: ATF-4 Rabbit mAb at 1/1000 dilution
Lane 1: NIH/3T3 whole cell lysate 20 µg
Lane 2: NIH/3T3 treated with Tunicamycin (2µg/mL, 8hr) whole cell lysate 20 µg
Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 38 kDa
Observed MW: 50 kDa
免疫细胞化学
ICC shows positive staining in HeLa cells treated with Tunicamycin (2µg/mL, 8hr). Anti- ATF-4 antibody was used at 1/100 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
Negative control：ICC shows weakly positive staining in HeLa cells untreated with Tunicamycin (2μg/mL, 8hr). Anti- ATF-4 antibody was used at 1/100 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
ChIP
Chromatin immunoprecipitation (ChIP) was performed on NIH/3T3+Tunicamycin (2µg/mL,8hr) cells cross - linked with 1% formaldehyde for 10 min, then chromatin was fragmented by sonication.
Parallel reactions used ATF-4 Recombinant Rabbit mAb (S-471-111) 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 ATF3 and SAT-α in ATF-4 Recombinant
Rabbit mAb (S-471-111)-immunoprecipitated sample.
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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