Phospho-c-Myc(Ser62) Antibody (YA211)

Phospho-c-Myc(Ser62) Antibody (YA211) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospho-c-Myc(Ser62).

C-MYC is a transcription factor that binds DNA non-specifically while also recognizing the core sequence 5'-CAC[GA]TG-3'. It activates the transcription of growth-related genes and binds to the VEGFA promoter to promote VEGFA production and sprouting angiogenesis. As a regulator of somatic reprogramming, it controls the self-renewal of embryonic stem cells (by similar). It functions with TAF6L to activate target gene expression through RNA polymerase II pause release (by similar). Additionally, it positively regulates the transcription of HNRNPA1, HNRNPA2, and PTBP1, which modulate the splicing of pyruvate kinase PKM by repressing exon 9 inclusion, leading to exon 10 inclusion and the production of the PKM M2 isoform.

Free

P01106

Predicted band size: 49 kDa; Observed band size: 57 kDa

Protein A affinity purified.

Nucleoplasm, nucleolus.

Non-conjugated

Phosphorylated

AB_3102584

Epigenetics and Nuclear Signaling

Primary Antibody; Recombinant Rabbit Monoclonal Antibody

Recombinant, Monoclonal

Rabbit

Human

WB: 1:500-1:2,000; IHC-P:1:50-1:200; ICC/IF: 1:50-1:200; IP: Use at an assay dependent concentration.

• 
  Western blot analysis of extracts from C6(lane 2(20μg) ,NIH/3T3(lane 3(20ug) using Phospho-c-Myc Antibody (HY-P80511) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
• 
  Immunocytochemistry analysis of Hela cells labelingPhospho-c-Myc(Ser62) with Phospho-c-Myc(Ser62)Antibody (HY-P80511) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 for 10 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with Phospho-c-Myc(Ser62)Antibody (HY-P80511) at 1/50 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L（HY-P8002, Green) 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. The Nuclear counterstain was DAPI (Blue).
• 
  Immunocytochemistry analysis of Hela cells labeling Phospho-c-Myc(Ser62) with Phospho-c-Myc(Ser62)Antibody (HY-P80511) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 for 10 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with Phospho-c-Myc(Ser62)Antibody (HY-P80511)at 1/100 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L（HY-P8002,Green) 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. The Nuclear counterstain was DAPI (Blue).
• 
  Immunohistochemical analysis of paraffin-embedded rat testis tissue using Phospho-c-Myc Antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked in QuickBlock for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/100 dilution in 4℃ overnight. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
• 
  Immunohistochemical analysis of paraffin-embedded rat testis tissue using Phospho-c-Myc Antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked in QuickBlock for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/100 dilution in 4℃ overnight. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

WB, ICC/IF, IHC-P, IP

Liquid

Supplied in 1*TBS (pH7.4), 0.05% BSA and 40% Glycerol. Preservative: 0.05% Sodium Azide.

Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

Shipping with blue ice.

IgG

Endogenous

Synthetic phosphopeptide corresponding to residues surrounding Ser62 of Human c-Myc.AA range:46-87.