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SMNDC1 is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. Zusätzlich bieten wir Ihnen SMNDC1 Proteine (12) und SMNDC1 Kits (4) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal SMNDC1 Primary Antibody für IP, WB - ABIN4354835
Giri, Shameer, Zimmermann, Saha, Chakraborty, Sharma, Arvizo, Madden, Mccormick, Kocher, Bhattacharya, Mukherjee: Understanding protein-nanoparticle interaction: a new gateway to disease therapeutics. in Bioconjugate chemistry 2014
The binding specificity and affinity of the Tudor domains of TDRD3 (zeige TDRD3 Antikörper), SMN (zeige STMN1 Antikörper) and SPF30 proteins were characterized quantitatively.
The structures of SMN (zeige STMN1 Antikörper) and SPF30 Tudor domains bound to symmetric and asymmetric dimethylated arginine (DMA (zeige HLA-DMA Antikörper)) are presented.
U2AF35 and hPrp3 interactions with SPF30 can occur simultaneously, thereby potentially linking 3' splice site recognition with tri-small nuclear ribonucleoprotein addition
This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.
Survival motor neuron domain-containing protein 1
, survival of motor neuron-related-splicing factor 30
, survival motor neuron domain containing 1
, 30 kDa splicing factor SMNrp
, SMN-related protein
, splicing factor 30, survival of motor neuron-related
, survival motor neuron domain-containing protein 1
, tudor domain containing 16C