RUNX2/CBFA1 Overexpression Lysate (Native) Summary
The lysate was created in HEK293T cells, using plasmid ID RC212884 and based on accession number NM_001024630. The protein contains a C-terminal DDK tag.
Homo sapiens runt-related transcription factor 2 (RUNX2), transcript variant 1, mRNA.
This product is intended for use as a positive control in Western Blot. You will receive the lysate (100ug), and an empty vector negative control (100 ug).
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Packaging, Storage & Formulations
Store at -80C. Avoid freeze-thaw cycles.
Lysate Details for RUNX2/CBFA1
HEK293T cells in 10-cm dishes were transiently transfected with a non-lipid polymer transfection reagent specially designed and manufactured for large volume DNA transfection. Transfected cells were cultured for 48hrs before collection. The cells were lysed in modified RIPA buffer (25mM Tris-HCl pH7.6, 150mM NaCl, 1% NP-40, 1mM EDTA, 1xProteinase inhibitor cocktail mix, 1mM PMSF and 1mM Na3VO4, and then centrifuged to clarify the lysate. Protein concentration was measured by BCA protein assay kit.This product is manufactured by and sold under license from OriGene Technologies and its use is limited solely for research purposes.
Alternate Names for RUNX2/CBFA1 Overexpression Lysate (Native)
- Acute myeloid leukemia 3 protein
- Core-binding factor subunit alpha-1
- PEA2-alpha A
- PEBP2-alpha A
- runt domain, alpha subunit 1
- runt-related transcription factor 2
- SL3/AKV core-binding factor alpha A subunit
- SL3-3 enhancer factor 1 alpha A subunit
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]. Transcript Variant: This variant (1) is the longer transcript of the two transcripts transcribed from promoter 1 (P1) and encodes the longer protein (isoform a) of these two transcripts. Isoform a is also referred to as the OSF2/CBFA1a isoform. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Lysates are guaranteed
for 6 months from date of receipt.
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Publications for RUNX2/CBFA1 Lysate (NBL1-15627) (0)
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FAQs for RUNX2/CBFA1 Lysate (NBL1-15627). (Showing 1 - 1 of 1 FAQ).
We would like an anti-RUNX2 for IHC-P which share cross reactivity with Rat, but not with Human.
- We don't have any data for our RUNX2 antibodies that confirms they will NOT detect the human protein. When we can confirm that an antibody will not react with a certain species, we display a (-) sign on the datasheet. Otherwise, if the species is not listed it means that it has not been tested.
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