Product Name	RUNX1T1
Chinese Name	周期素D相关蛋白抗体
Alias	Acute myelogenous leukemia 1 translocation 1 cyclin D related; Acute myelogenous leukemia 1 translocation 1 protein; AML1T1; CBFA2T1; CDR; Core binding factor runt domain alpha subunit 2 translocated to 1; Core binding factor runt domain alpha subunit 2 translocated to 1 cyclin D related; Cyclin D related; Cyclin D related protein; Eight twenty one protein; Eigth twenty one protein; ETO; ETO protein; MTG 8; MTG 8b; MTG8. MTG8 protein; MTG8b antibody Myeloid translocation gene on 8q22; Protein CBFA2T1; Protein ETO; Protein MTG 8; Protein MTG8; Runt related transcription factor 1 translocated to 1 (cyclin D related); Runt related transcription factor 1 translocated to 1; Runt related transcription factor 1 translocated to 1 cyclin D related; Zinc finger MYND domain containing protein 2; ZMYND 2; ZMYND2.
Research Area	Tumour  Cell biology  Chromatin and nuclear signals  Signal transduction  Cyclin
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	Mouse,  (predicted: Human, Rat, Chicken, Dog, Pig, Horse, Rabbit, )
Applications	WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 （Paraffin sections need antigen repair） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight	66kDa
Cellular localization	The nucleus
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human RUNX1T1/ETO: 431-530/604
Lsotype	IgG
Purification	affinity purified by Protein A
Buffer Solution	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed	PubMed
Product Detail	RUNX1T1 is a putative zinc finger transcription factor and oncoprotein. In acute myeloid leukemia, especially in the M2 subtype, the t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities. The translocation produces a chimeric gene made up of the 5'-region of the RUNX1 gene fused to the 3'-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Several transcript variants encoding multiple isoforms have been found for this gene. Subunit: Homotetramer. Heterotetramer with CBFA2T2 and CBFA2T3. Interacts with TCF12, SIN3A, HDAC1, HDAC2, HDAC3, NCOR1 and NCOR2. Interacts with ATN1 (via its N-terminus); the interaction enhances the transcriptional repression. Subcellular Location: Nucleus. Tissue Specificity: Most abundantly expressed in brain. Lower levels in lung, heart, testis and ovary. Similarity: Belongs to the CBFA2T family. Contains 1 MYND-type zinc finger. Contains 1 TAFH (NHR1) domain. SWISS: Q06455 Gene ID: 862 Database links: Entrez Gene: 862 Human Entrez Gene: 12395 Mouse Entrez Gene: 362489 Rat Omim: 133435 Human SwissProt: Q06455 Human SwissProt: Q61909 Mouse Unigene: 368431 Human Unigene: 470961 Mouse Unigene: 4909 Mouse Unigene: 218117 Rat
Product Picture	Sample: Brain (Mouse) Lysate at 40 ug Primary: Anti-RUNX1T1 (SL6101R) at 1/300 dilution Secondary: HRP conjugated Goat-Anti-rabbit IgG (SL0295G-HRP) at 1/5000 dilution Predicted band size: 66 kD Observed band size: 66 kD

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