ID3 Mouse Monoclonal Antibody [Clone ID: OTI7B6]

CAT#: TA500811

Anti-ID3 mouse monoclonal antibody, clone OTI7B6 (formerly 7B6)

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY ID3 (RC200583, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-ID3. Positive lysates LY419492 (100ug) and LC419492 (20ug) can be purchased separately from OriGene.

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  Immunohistochemical staining of paraffin-embedded Kidney tissue within the normal limits using anti-ID3mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100°C for 10min, TA500811, Dilution 1:50)

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  Anti-ID3 mouse monoclonal antibody (TA500811) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY ID3 (RC200583).

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  Immunofluorescent staining of HeLa cells using anti-ID3 mouse monoclonal antibody (TA500811).

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  Immunofluorescent staining of HT29 cells using anti-ID3 mouse monoclonal antibody (TA500811).

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Specifications

Product Data

• Clone Name: OTI7B6
• Applications: IF, IHC, WB
• Recommended Dilution: WB 1:2000, IHC 1:50, IF 1:100
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human ID3 (NP_002158) produced in HEK293T cell.
• Formulation: PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
• Concentration: 0.75 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Unconjugated
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 13.0 kDa
• Gene Name: inhibitor of DNA binding 3, HLH protein
• Database Link:
  NP_002158
  Entrez Gene 3399 Human
  UniProt ID Q02535
• Background: This gene encodes a protein belonging to the raf/mil family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERKs signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene are associated with cardiofaciocutaneous syndrome, a disease characterized by heart defects, mental retardation and a distinctive facial appearance. Mutations in this gene have also been associated with various cancers, including non-Hodgkin lymphoma, colorectal cancer, malignant melanoma, thyroid carcinoma, non-small cell lung carcinoma, and adenocarcinoma of lung. A pseudogene, which is located on chromosome X, has been identified for this gene.
• Synonyms: bHLHb25; HEIR-1

Reference Data

• Protein Families: Druggable Genome, ES Cell Differentiation/IPS, Transcription Factors
• Protein Pathways: TGF-beta signaling pathway