
Thermo Fisher Scientific RUNX1T1 Monoclonal Antibody (5A12)
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Applications
Tested Dilution
Publications
Western Blot (WB)
1-5 µg/mL
Immunocytochemistry (ICC/IF)
10 µg/mL
ELISA (ELISA)
0.3 ng/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2a, kappa
Class
Monoclonal
Type
Antibody
Clone
5A12
Immunogen
RUNX1T1 (NP_004340, 416 a.a. approximately 525 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
RUNX1T1,
uniProtId:
Q06455-1,
ncbiNodeId:
9606,
antigenRange:
416-525,
antigenLength:
604,
antigenImageFileName:
H00000862-M01_RUNX1T1_Q06455-1_House_mouse.svg,
antigenImageFileNamePDP:
H00000862-M01_RUNX1T1_Q06455-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
See Label
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.4
Contains
no preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
Sequence of this protein is as follows: EEIWKKAEEA VNEVKRQAMT ELQKAVSEAE RKAHDMITTE RAKMERTVAE AKRQAAEDAL AVINQQEDSS ESCWNCGRKA SETCSGCNTA RYCGSFCQHK DWEKHHHICG
Target Information
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. The protein encoded by this gene 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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