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c-Myc [6G6]

c-Myc [6G6]

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基础信息
存储条件
产品详情
Product Profile
Product Namec-Myc [6G6]
Antibody TypePrimary Antibodies
Antigen AliasAU016757 antibody 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 protein antibody Myc proto oncogene protein antibody Myc proto-oncogene protein antibody myc-related translation/localization regulatory factor antibody MYC_HUMAN antibody Myc2 antibody MYCC antibody Myelocytomatosis oncogene antibody Niard antibody Nird antibody Oncogene Myc antibody OTTHUMP00000158589 antibody Proto-oncogene c-Myc antibody Protooncogene homologous to myelocytomatosis virus antibody RNCMYC antibody Transcription factor p64 antibody Transcriptional regulator Myc-A antibody V-Myc avian myelocytomatosis viral oncogene homolog antibody v-myc myelocytomatosis viral oncogene homolog (avian) antibody
Product descriptionC-Myc-, N-Myc- and L-Myc-encoded proteins function in cell proliferation, differentiation and neoplastic disease. Myc proteins are nuclear proteins with relatively short half lives. Amplification of the c-Myc gene has been found in several types of human tumors including lung, breast and colon carcinomas, while the N-Myc gene has been found amplified in neuroblastomas. The L-Myc gene has been reported to be amplified and expressed at high level in human small cell lung carcinomas. The presence of three sequence motifs in the c-Myc COOH terminus, including the leucine zipper, the helix-loop-helix and a basic region provided initial evidence for a sequence-specific binding function. A basic region helix-loop-helix leucine zipper motif (bHLH-Zip) protein, designated Max, specifically associates with c-Myc, N-Myc and L-Myc proteins. The Myc-Max complex binds to DNA in a sequence-specific manner under conditions where neither Max nor Myc exhibit appreciable binding. Max can also form heterodimers with at least two additional bHLH-Zip proteins, Mad and Mxi1, and Mad-Max dimers have been shown to repress transcription through interaction with mSin3.
Immunogenpeptide
Key Feature
ClonalityMonoclonal
IsotypeIgG1
Host SpeciesMouse
Tested ApplicationsWBIPIFIHC-PFCM

WB:1:100-1:1,000
IP:1-2 μg per 100-500 μg of total protein(1 ml of cell lysate)
IF:1:50-1:500
IHC:1:50-1:500 FCM
Species ReactivityHumanMouseRatMonkey
Concentration2mg/ml
Target Information
Alternative NamesAU016757 antibody
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 protein antibody
Myc proto oncogene protein antibody
Myc proto-oncogene protein antibody
myc-related translation/localization regulatory factor antibody
MYC_HUMAN antibody
Myc2 antibody
MYCC antibody
Myelocytomatosis oncogene antibody
Niard antibody
Nird antibody
Oncogene Myc antibody
OTTHUMP00000158589 antibody
Proto-oncogene c-Myc antibody
Protooncogene homologous to myelocytomatosis virus antibody
RNCMYC antibody
Transcription factor p64 antibody
Transcriptional regulator Myc-A antibody
V-Myc avian myelocytomatosis viral oncogene homolog antibody
v-myc myelocytomatosis viral oncogene homolog (avian) antibody
Molecular Weight(MW)67kDa
Cellular LocalizationNucleus
Database Links
SwissProt IDP01106
Application

Application

Fig1: Westernblot analysis of c-Myc expressionin untreated (A) and (E)-4-Hydroxyhexenal treated (B) Jurkat whole cell lysates. Note down-regulation of c-Myc in lane B.

Application

Fig2: Immunoperoxidase staining of formalin-fixed, paraffin-embedded normal human colon showing intense nuclear staining (A). Immunofluorescence staining of methanol-fixed COS cells transfected with c-Myc fusion protein showing cytoplasmic staining (B).
Positive ControlJurkat, COS
Application NotesWB:1:100-1:1,000
IP:1-2 μg per 100-500 μg of total protein(1 ml of cell lysate)
IF:1:50-1:500
IHC:1:50-1:500 FCM
Additional Information
FormLiquid
Storage InstructionsStore at +4℃
Storage Buffer1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.


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