概述
产品名称
Myc tag Rabbit Polyclonal Antibody
抗体类型
Rabbit Polyclonal Antibody
免疫原
Synthetic peptide within human Myc aa 410-420.
种属反应性
Species independent
验证应用
WB, IP, IF-Cell, FC
阳性对照
PG-CM cell lysates, C-terminal Myc-tagged recombinant protein, N-terminal Myc-tagged recombinant protein.
偶联
unconjugated
RRID
产品特性
形态
Liquid
浓度
1ug/ul
存放说明
Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
存储缓冲液
1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
亚型
IgG
纯化方式
Immunogen affinity purified.
应用稀释度
-
WB
-
1:1,000-1:2,000
-
IP
-
2-5 µg/ml.
-
IF-Cell
-
1:200
-
FC
-
1:1,000
发表文章中的应用
发表文章中的种属
Human | See 30 publications below |
Chicken | See 3 publications below |
Pig | See 3 publications below |
靶点
功能
Myc gene encodes for a transcription factor that is believed to regulate expression of 15% of all genes through binding on Enhancer Box sequences (E-boxes) and recruiting histone acetyltransferases (HATs). c-Myc is commonly activated in a variety of tumor cells and plays an important role in cellular proliferation, differentiation, apoptosis and cell cycle progression. This Myc-Tag antibody detects Myc-tagged fusion proteins.
背景文献
1. "A quantitative atlas of mitotic phosphorylation."Dephoure N., Zhou C., Villen J., Beausoleil S.A., Bakalarski C.E., Elledge S.J., Gygi S.P.Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008)
2. "Transactivation of gene expression by Myc is inhibited by mutation at the phosphorylation sites Thr-58 and Ser-62."Gupta S., Seth A., Davis R.J. Proc. Natl. Acad. Sci. U.S.A. 90:3216-3220(1993)
翻译后修饰
Phosphorylated by PRKDC. Phosphorylation at Ser-329 by PIM2 leads to the stabilization of MYC (By similarity). Phosphorylation at Ser-62 by CDK2 prevents Ras-induced senescence. Phosphorylated at Ser-62 by DYRK2; this primes the protein for subsequent phosphorylation by GSK3B at Thr-58. Phosphorylation at Thr-58 and Ser-62 by GSK3 is required for ubiquitination and degradation by the proteasome.; Ubiquitinated by the SCF(FBXW7) complex when phosphorylated at Thr-58 and Ser-62, leading to its degradation by the proteasome. In the nucleoplasm, ubiquitination is counteracted by USP28, which interacts with isoform 1 of FBXW7 (FBW7alpha), leading to its deubiquitination and preventing degradation. In the nucleolus, however, ubiquitination is not counteracted by USP28 but by USP36, due to the lack of interaction between isoform 3 of FBXW7 (FBW7gamma) and USP28, explaining the selective MYC degradation in the nucleolus. Also polyubiquitinated by the DCX(TRUSS) complex. Ubiquitinated by TRIM6 in a phosphorylation-independent manner (By similarity).
UNIPROT #
别名
avian myelocytomatosis viral oncogene homolog antibody
bHLHe39 antibody
c-Myc antibody
class E basic helix-loop-helix protein 39 antibody
MRTL antibody
MYC antibody
Myc Epitope Tag antibody
myc proto-oncogene protein antibody
myc-related translation/localization regulatory factor antibody
oncogene c-Myc antibody
展开avian myelocytomatosis viral oncogene homolog antibody
bHLHe39 antibody
c-Myc antibody
class E basic helix-loop-helix protein 39 antibody
MRTL antibody
MYC antibody
Myc Epitope Tag antibody
myc proto-oncogene protein antibody
myc-related translation/localization regulatory factor antibody
oncogene c-Myc antibody
proto-oncogene c-Myc antibody
protooncogene homologous to myelocytomatosis virus antibody
transcription factor p64 antibody
v-myc avian myelocytomatosis viral oncogene homolog antibody
v-myc myelocytomatosis viral oncogene homolog (avian) antibody
折叠图片
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Western blot analysis of Myc tag on PG-CM lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (R1208-1, 1/1,000) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
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Western blot analysis of Myc tag on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (R1208-1, 1/1,000) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: C-terminal Myc-tagged recombinant protein
Lane 2: N-terminal Myc-tagged recombinant protein -
Myc tag was immunoprecipitated in 2µg C terminal Myc Tag fusion protein lysate with R1208-1 at 2 µg/20 µl agarose. Western blot was performed from the immunoprecipitate using EM31105 at 1/1000 dilution. Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:20,000 dilution was used for 60 mins at room temperature.
Lane 1: Myc Tag fusion protein lysate (input).
Lane 2: R1208-1 IP in Myc Tag fusion protein lysate.
Lane 3: Rabbit IgG instead of R1208-1 in Myc Tag fusion protein lysate.
Blocking/Dilution buffer: 5% NFDM/TBST -
Myc tag was immunoprecipitated in 2µg N terminal Myc Tag fusion protein lysate with R1208-1 at 2 µg/20 µl agarose. Western blot was performed from the immunoprecipitate using EM31105 at 1/1000 dilution. Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:20,000 dilution was used for 60 mins at room temperature.
Lane 1: Myc Tag fusion protein lysate (input).
Lane 2: R1208-1 IP in Myc Tag fusion protein lysate.
Lane 3: Rabbit IgG instead of R1208-1 in Myc Tag fusion protein lysate.
Blocking/Dilution buffer: 5% NFDM/TBST -
Immunocytochemistry analysis of 293T cells labeling Myc tag with Rabbit anti-Myc tag antibody (R1208-1) at 1/200 dilution.
293T cells, transfected with Myc-tagged empty control, Claudin18.2 (C-terminal) or Histone H3.1 (N-terminal) expression vector, respectively, were fixed in 4% paraformaldehyde for 10 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Myc tag antibody (R1208-1) at 1/200 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594, HA1122) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
Myc Tag (HA601081, green) was stained at 1/1,000 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) was used as the secondary antibody at 1/1,000 dilution. -
Flow cytometric analysis of 293T cells transfected C-myc-tag labeling Myc tag.
Cells were fixed and permeabilized. Then stained with the primary antibody (R1208-1, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
引文
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Characterization and functional analysis of chicken promyelocytic leukemia protein
Author: Wang Shengnan,et al
PMID: NO PMID20240903
应用: WB
反应种属: Human
发表时间: 2024 Sep
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Bipartite nuclear localization sequence is indispensable for nuclear import and stability of self-dimerization of ADARa in Bombyx mori
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应用: WB
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发表时间: 2024 Oct
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Decoupling actin assembly from microtubule disassembly by TBC1D3C-mediated direct GEF-H1 activation
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应用: WB
反应种属: Human
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E3 ubiquitin ligase UBR5 modulates circadian rhythm by facilitating the ubiquitination and degradation of the key clock transcription factor BMAL1
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应用: WB,IP
反应种属: Human
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An H3K14 ubiquitination-dependent SUV39H recruitment and activation is uniquely required for mammalian pericentromeric heterochromatin formation
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KPNA3 regulates histone locus body formation by modulating condensation and nuclear import of NPAT
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SUMO1 Modification Facilitates Avibirnavirus Replication by Stabilizing Polymerase VP1. Journal of virology, 93(10), e02227-18.
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TP53INP2 contributes to autophagosome formation by promoting LC3-ATG7 interaction
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p73 coordinates with Δ133p53 to promote DNA double-strand break repair
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Acetylation accumulates PFKFB3 in cytoplasm to promote glycolysis and protects cells from cisplatin-induced apoptosis
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Caspase-Dependent Apoptosis Induction via Viral Protein ORF4 of Porcine Circovirus 2 Binding to Mitochondrial Adenine Nucleotide Translocase 3
Author: Jiyong Zhou
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应用: WB
反应种属: Porcine Circovirus
发表时间: 2018 Apr
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SIRT7 deacetylates DDB1 and suppresses the activity of the CRL4 E3 ligase complexes. The FEBS journal, 284(21), 3619–3636.
Author: Mo, Y., Lin, R., Liu, P., Tan, M., Xiong, Y., Guan, K. L., & Yuan, H. X.
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Bile Acids Control Inflammation and Metabolic Disorder through Inhibition of NLRP3 Inflammasome
Author: Di Wang
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应用: WB
反应种属: Human
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The co-chaperone Cdc37 regulates the rabies virus phosphoprotein stability by targeting to Hsp90AA1 machinery
Author: Jiyong Zhou
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应用: WB
反应种属: Mouse
发表时间: 2016 Jun
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Circovirus Transport Proceeds via Direct Interaction of the Cytoplasmic Dynein IC1 Subunit with theViral Capsid Protein
Author: Jiyong Zhou
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应用: WB,IP
反应种属: Circovirus
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PARD3 induces TAZ activation and cell growth by promoting LATS1 and PP1 interaction
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Citation
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Identification of 17 HrpX-Regulated Proteins Including Two Novel Type III Effectors,XOC_3956 and XOC_1550,in Xanthomonas oryzae pv. oryzicola
Author: Gong-you Chen
PMID: 24675748
应用: WB
反应种属: Xanthomonas oryzae pv. oryzicola
发表时间: 2014 Mar
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Citation