BMP4 Human shRNA Plasmid Kit (Locus ID 652)

Specifications

Product Data
Locus ID	652
Synonyms	BMP2B; BMP2B1; MCOPS6; OFC11; ZYME
Vector	pGFP-V-RS
E. coli Selection	Kanamycin
Mammalian Cell Selection	Puromycin
Format	Retroviral plasmids
Kit Components	BMP4 - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 652). 5µg purified plasmid DNA per construct 29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free.
RefSeq	NM_001202, NM_130850, NM_130851, NM_001347912, NM_001347913, NM_001347914, NM_001347915, NM_001347916, NM_001347917, NM_001202.1, NM_001202.2, NM_001202.3, NM_001202.4, NM_001202.5, NM_130850.1, NM_130850.2, NM_130850.3, NM_130850.4, NM_130851.1, NM_130851.2, NM_130851.3, BC020546, BC020546.2
UniProt ID	P12644
Summary	This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein regulates heart development and adipogenesis. Mutations in this gene are associated with orofacial cleft and microphthalmia in human patients. The encoded protein may also be involved in the pathology of multiple cardiovascular diseases and human cancers. [provided by RefSeq, Jul 2016]
shRNA Design	These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact tech@biotrend.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service.
Performance Guaranteed	OriGene guarantees that the sequences in the shRNA expression cassettes are verified to correspond to the target gene with 100% identity. One of the four constructs at minimum are guaranteed to produce 70% or more gene expression knock-down provided a minimum transfection efficiency of 80% is achieved. Western Blot data is recommended over qPCR to evaluate the silencing effect of the shRNA constructs 72 hrs post transfection. To properly assess knockdown, the gene expression level from the included scramble control vector must be used in comparison with the target-specific shRNA transfected samples. For non-conforming shRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the shRNA kit. To arrange for a free replacement with newly designed constructs, please contact Technical Services at tech@biotrend.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled shRNA control (Western Blot data preferred).