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Defects in ETFDH are responsible for an autosomal recessive disorder of amino acid
nucleocapsid phosphoprotein
This protein is cell-cycle regulated and is required for chromatin-induced microtubule stabilization and spindle formation
miRNA and siRNA) and modified nucleic acids (antisense oligonucleotides)
Recombinant human TRAIL/Apo2L (rhTRAIL) produced in E
REPIN1 Polyclonal Antibody-BS77740 Size:100µl Defects in ETFDH are responsibleREPIN1 Polyclonal Antibody Sizes: 50l, 100l Catalogue Numbers: BS77740 50, BS77740 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: Q9BWE0 Host: Rabbit Reactivity: Human, Mouse Applications: WB All Applications: WB,1: 500 1: 2000 Background: Sequence specific double stranded DNA binding protein required for initiation of chromosomal DNA replication. Binds on 5' ATT 3' reiterated sequences downstream of the origin
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