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Runt Related Transcription Factor 2 (RUNX2), Recombinant Protein

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產(chǎn)品名稱: Runt Related Transcription Factor 2 (RUNX2), Recombinant Protein
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Runt Related Transcription Factor 2 (RUNX2), Recombinant Protein


Runt Related Transcription Factor 2 (RUNX2), Recombinant Protein  的詳細(xì)介紹
Product Name

Runt Related Transcription Factor 2 (RUNX2), Recombinant Protein

Popular Item
Full Product Name

Recombinant Runt Related Transcription Factor 2 (RUNX2)

Product Gene Name

RUNX2 recombinant protein

[Similar Products]
Matching Pairs
Unconjugated Antibody: Runt Related Transcription Factor 2 (RUNX2) (MBS2006848)
Immunogen: Runt Related Transcription Factor 2 (RUNX2) (MBS2012302)
Matching Pairs
APC-CY7 Conjugated Antibody: Runt Related Transcription Factor 2 (RUNX2) (MBS2050442)
Immunogen: Runt Related Transcription Factor 2 (RUNX2) (MBS2012302)
Matching Pairs
PE Conjugated Antibody: Runt Related Transcription Factor 2 (RUNX2) (MBS2050443)
Immunogen: Runt Related Transcription Factor 2 (RUNX2) (MBS2012302)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Chromosome Location
Chromosome: 6; NC_000006.11 (45296054..45518819). Location: 6p21
OMIM
119600
3D Structure
ModBase 3D Structure for Q13950
Host
E.coli
Species Reactivity
Homo sapiens (Human)
Purity/Purification
> 90%
Form/Format
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
Source
Prokaryotic expression
Residues
Tyr299~Tyr521
Tags
N-terminal His Tag
Subcellular Location
Nucleus
Traits
Freeze-dried powder
Predicted isoelectric point
6.4
Predicted Molecular Mass
25.3kDa
Accurate Molecular Mass
26kDa as determined by SDS-PAGE reducing conditions.
Usage
Reconstitute in 10mM PBS (pH7.4) to a concentration of 0.1-1.0 mg/mL. Do not vortex.
Preparation and Storage
Storage: Avoid repeated freeze/thaw cycles.
Store at 2-8oC for one month.
Aliquot and store at -80oC for 12 months.

Stability Test: The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
ISO Certification
Manufactured in an ISO 9001:2008 and ISO 13485:2003 Certified Laboratory.
Supply Chain Verification
Manufactured in a lab with traceable raw materials. Bulk orders can typically be prepared to the customera??s specifications, please inquire.
Other Notes
Small volumes of RUNX2 recombinant protein vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Applications Tested/Suitable for RUNX2 recombinant protein
Positive Control, Immunogen, SDS-PAGE, WB.
(May be suitable for use in other assays to be determined by the end user.)

SDS-Page of RUNX2 recombinant protein
RUNX2 recombinant protein SDS-Page image
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NCBI/Uniprot data below describe general gene information for RUNX2. It may not necessarily be applicable to this product.
NCBI GI #
226442791
NCBI GeneID
860
NCBI Accession #
NP_001015051.3 [Other Products]
NCBI GenBank Nucleotide #
NM_001015051.3 [Other Products]
UniProt Primary Accession #
Q13950 [Other Products]
UniProt Secondary Accession #
O14614; O14615; O95181[Other Products]
UniProt Related Accession #
Q13950[Other Products]
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NCBI Official Full Name
runt-related transcription factor 2 isoform b
NCBI Official Synonym Full Names
runt-related transcription factor 2
NCBI Official Symbol
RUNX2??[Similar Products]
NCBI Official Synonym Symbols
CCD; AML3; CCD1; CLCD; OSF2; CBFA1; OSF-2; PEA2aA; PEBP2aA; CBF-alpha-1
??[Similar Products]
NCBI Protein Information
runt-related transcription factor 2; PEA2-alpha A; PEBP2-alpha A; oncogene AML-3; acute myeloid leukemia 3 protein; SL3-3 enhancer factor 1 alpha A subunit; osteoblast-specific transcription factor 2; SL3/AKV core-binding factor alpha A subunit; core-binding factor, runt domain, alpha subunit 1; polyomavirus enhancer-binding protein 2 alpha A subunit
UniProt Protein Name
Runt-related transcription factor 2
UniProt Synonym Protein Names
Acute myeloid leukemia 3 protein; Core-binding factor subunit alpha-1; CBF-alpha-1; Oncogene AML-3; Osteoblast-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
Protein Family
Runt-related transcription factor
UniProt Gene Name
RUNX2??[Similar Products]
UniProt Synonym Gene Names
AML3; CBFA1; OSF2; PEBP2A; CBF-alpha-1; OSF-2; PEA2-alpha A??[Similar Products]
UniProt Entry Name
RUNX2_HUMAN
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NCBI Summary for RUNX2
This 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. 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 2008]
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UniProt Comments for RUNX2
AML3: Transcription factor involved in osteoblastic differentiation and skeletal morphogenesis. Essential for the maturation of osteoblasts and both intramembranous and endochondral ossification. CBF binds to the core site, 5'- PYGPYGGT-3', of a number of enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers, osteocalcin, osteopontin, bone sialoprotein, alpha 1(I) collagen, LCK, IL-3 and GM-CSF promoters. In osteoblasts, supports transcription activation: synergizes with SPEN/MINT to enhance FGFR2-mediated activation of the osteocalcin FGF-responsive element (OCFRE). Inhibits KAT6B-dependent transcriptional activation. Interaction with SATB2 results in enhanced DNA binding and transactivation by these transcription factors. Heterodimer of an alpha and a beta subunit. Interacts with HIVEP3 and HIPK3. The alpha subunit binds DNA as a monomer and through the Runt domain. DNA-binding is increased by heterodimerization. Interacts with XRCC6 (Ku70) and XRCC5 (Ku80). Interacts with KAT6A and KAT6B. Binds to cyclin B1 CCNB1. Interacts with DDX5. Specifically expressed in osteoblasts. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: DNA-binding; Transcription factor

Chromosomal Location of Human Ortholog: 6p21

Cellular Component: nucleoplasm; transcription factor complex; nuclear chromatin; cytoplasm

Molecular Function: protein domain specific binding; protein binding; bHLH transcription factor binding; chromatin binding; transcription factor activity; ATP binding

Biological Process: embryonic forelimb morphogenesis; transcription initiation from RNA polymerase II promoter; ossification; positive regulation of transcription, DNA-dependent; cell maturation; regulation of fibroblast growth factor receptor signaling pathway; chondrocyte development; stem cell differentiation; embryonic cranial skeleton morphogenesis; odontogenesis of dentine-containing teeth; osteoblast development; osteoblast differentiation; BMP signaling pathway; positive regulation of osteoblast differentiation; positive regulation of chondrocyte differentiation; negative regulation of smoothened signaling pathway; positive regulation of cell proliferation; gene expression; negative regulation of transcription, DNA-dependent; T cell differentiation; regulation of odontogenesis of dentine-containing teeth; endochondral ossification; osteoblast fate commitment

Disease: Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly; Cleidocranial Dysplasia
Research Articles on RUNX2
1. RUNX2 has a primary role in the differentiation of osteoblasts, hypertrophy of cartilage at the growth plate, cell migration, and vascular invasion of bone. RUNX2 mutations cause cleidocranial dysplasia.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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