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OriGene cDNAs in recent publications

BAT3 and SET1A form a complex with CTCFL/BORIS to modulate H3K4 histone dimethylation and gene expression,  Mol. Cell. Biol. Nov.2008; 28(21): p. 6720-6729 [BAT3]

Heme Oxygenase-1 Regulates Cardiac Mitochondrial Biogenesis via Nrf2-Mediated Transcriptional Control of Nuclear Respiratory Factor-1, Circ. Res., Oct 2008; 10.1161/01.RES.0000338597.71702.ad. [AKT1]

Interactions of S100A2 and S100A6 with the Tetratricopeptide Repeat Proteins, Hsp90/Hsp70-organizing Protein and Kinesin Light Chain,  J. Biol. Chem., Oct 2008; 283: 28246 - 28258. [TOR1A]

Significance of Organic Cation Transporter 3 (SLC22A3) Expression for the Cytotoxic Effect of Oxaliplatin in Colorectal Cancer, Drug Metab. Dispos., Nov 2008; 36: 2299 - 2306. [POU5F1(OCT3)]

Stroma-dependent apoptosis in clonal hematopoietic precursors correlates with expression of PYCARD Blood, Oct 2008; 10.1182/blood-2008-04-152686. [TNFRSF1A] 

TRUECLONE COLLECTION

Cat. No. Ref. ID Description Delivery
SC115442 NM_000061 Homo sapiens Bruton agammaglobulinemia tyrosine kinase (BTK) as transfection-ready DNA NM_000061.1 Immediate
Functional Details
Larger aliquots of this purified plasmid are available on the next page. For 50 ug and 100 ug orders, delivery will take four additional weeks from the estimated delivery time.


Potent 29-mer shRNA Available
Open Reading Frame Clones
Optimal Transfection Reagent
Antibody Search Option


Researchers who bought this clone have also purchased:
Western Blotting Reagents
• MYC/DDK Tagged Western Blot Molecular Weight Markers
• Anti-tag antibodies
• HRP-Conjugated secondary antibodies and Western blot reagents
Insert Size determined experimentally by digestion of the clone with Not I restriction enzyme

Reference Data

Family: Kinase

RefSeq Size: 2591

RefSeq ORF: 1980

RefSeq: NM_000061.1, NP_000052
LocusID: 695
Cytogenetic: Xq21.33
Domains: pkinase, SH2, TyrKc, SH3, BTK, PH, S_TKc
Summary: Defects in the Bruton tyrosine kinase (BTK) gene cause Agammaglobulinemia. Agammaglobulinemia is an X-linked immunodeficiency characterized by failure to produce mature B lymphocyte cells and associated with a failure of Ig heavy chain rearrangement. [provided by RefSeq].


family Pathway Function

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