RUNX2 rabbit pAb

RUNX2 rabbit pAb

AO-06-ES4086-100

RUNX2 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4086
Product nameRUNX2 rabbit pAb
ReactivityHuman;Mouse;Rat;Dog
ApplicationsIF;WB;ELISA
Other nameRUNX2; AML3; CBFA1; OSF2; PEBP2A; Runt-related transcription factor 2; Acute myeloid leukemia 3 protein; Core-binding factor subunit alpha-1; CBF-alpha-1; Oncogene AML-3Osteoblast-specific transcription factor 2; OSF-2; Polyomavirus enhancer-binding protein 2 alpha A subunit; PEA2-alpha A; PEBP2-alpha A; SL3-3 enhancer factor 1 alpha A subunit; SL3/AKV core-binding factor alpha A subunit
Size100μL
Unit price ($)248
Human gene ID860
Human Swiss-ProtQ13950
SourceRabbit
IsotypeIgG
TargetRUNX2
Fields>>Parathyroid hormone synthesis, secretion and action;>>Transcriptional misregulation in cancer
Gene nameRUNX2
Protein nameRunt-related transcription factor 2
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID12393
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ08775
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-ProtQ9Z2J9
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from the Internal region of human RUNX2. AA range:201-250
SpecificityRUNX2 Polyclonal Antibody detects endogenous levels of RUNX2 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionIF: 1:50-200 Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)56kD
BackgroundThis gene is a member of the RUNX family of transcription factors and encodes a nuclear protein with an Runt DNA-binding domain. This protein is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can bind DNA both as a monomer or, with more affinity, as a subunit of a heterodimeric complex. Two regions of potential trinucleotide repeat expansions are present in the N-terminal region of the encoded protein, and these and other mutations in this gene have been associated with the bone development disorder cleidocranial dysplasia (CCD). Transcript variants that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing. [provided by RefSeq, Jul 2016],
Functiondisease:Defects in RUNX2 are the cause of cleidocranial dysplasia (CCD) [MIM:119600]. CCD is an autosomal dominant skeletal disorder with high penetrance and variable expressivity. It is due to defective endochondral and intramembranous bone formation. Typical features include hypoplasia/aplasia of clavicles, patent fontanelles, wormian bones (additional cranial plates caused by abnormal ossification of the calvaria), supernumerary teeth, short stature, and other skeletal changes. In some cases defects in RUNX2 are exclusively associated with dental anomalies.,domain:A proline/serine/threonine rich region at the C-terminus is necessary for transcriptional activation of target genes and contains the phosphorylation sites.,function:Transcription factor involved in osteoblastic differentiation and skeletal morphogenesis. Essential for the maturation of osteoblasts and both intramembranous a
Subcellular locationNucleus .
ExpressionSpecifically expressed in osteoblasts.

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: AO-06-ES4086-100
: 10 Produits
Hurry! only 10 items left in stock.

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