Human SMNDC1 Recombinant Protein (RPPB4719)

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SKU:
RPPB4719
Product type:
Recombinant Protein
Size:
10ug
Species:
Human
Target:
SMNDC1
Synonyms:
SMNR
Synonyms:
SMN-related protein
Synonyms:
SPF30
Synonyms:
Survival Motor Neuron Domain Containing 1
Source:
Escherichia Coli
Uniprot:
O75940
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Description

Product Name:Human SMNDC1 Recombinant Protein
Product Code:RPPB4719
Size:10µg
Species:Human
Target:SMNDC1
Synonyms:SMNR, SMN-related protein, SPF30, Survival Motor Neuron Domain Containing 1, 30kDa Splicing Factor SMNrp, Splicing Factor 30, Survival of Motor Neuron-related.
Source:Escherichia Coli
Physical Appearance:Sterile Filtered clear solution.
Formulation:The SMNDC1 protein solution (0.5mg/1ml) is formulated in 20mM Tris-HCl buffer (pH8.0) 1mM DTT, 100mM NaCl and 10% glycerol.
Stability:Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time.Please avoid freeze thaw cycles.
Purity:Greater than 90% as determined by SDS-PAGE.
Amino Acid Sequence:MGSSHHHHHH SSGLVPRGSH MSEDLAKQLA SYKAQLQQVE AALSGNGENE DLLKLKKDLQ EVIELTKDLL STQPSETLAS SDSFASTQPT HSWKVGDKCM AVWSEDGQCY EAEIEEIDEE NGTAAITFAG YGNAEVTPLL NLKPVEEGRK AKEDSGNKPM SKKEMIAQQR EYKKKKALKK AQRIKELEQE REDQKVKWQQ FNNRAYSKNK KGQVKRSIFA SPESVTGKVG VGTCGIADKP MTQYQDTSKY NVRHLMPQ

SMNDC1 is a vital splicing factor obligatory for spliceosome assembly which is a part of the SMN family. SMNDC1 has one Tudor domain with significant similarity to Survival Motor Neuron (SMN) and is expressed in heart, pancreas and skeletal muscle, localizing to Cajal bodies and nuclear speckles. Mutations in SMNDC1 are cause of autosomal recessive proximal spinal muscular atrophy.

SMNDC1 produced in E.Coli is a single, non-glycosylated polypeptide chain containing 258 amino acids (1-238a.a.) and having a molecular mass of 28.9kDa.SMNDC1 is fused to a 20 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.

UniProt Protein Function:SPF30: Necessary for spliceosome assembly. Overexpression causes apoptosis. Belongs to the SMN family.
UniProt Protein Details:

Protein type:Spliceosome; RNA processing; RNA splicing; RNA-binding

Chromosomal Location of Human Ortholog: 10q23

Cellular Component: nucleoplasm; spliceosome; Cajal body; intermediate filament cytoskeleton; cytoplasm; nuclear speck; nucleus

Molecular Function:protein binding

Biological Process: RNA splicing, via transesterification reactions; apoptosis; RNA splicing; spliceosome assembly; mRNA processing

NCBI Summary: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. [provided by RefSeq, Jul 2008]
UniProt Code:O75940
NCBI GenInfo Identifier:37087924
NCBI Gene ID:10285
NCBI Accession:O75940.1
UniProt Related Accession:O75940
Molecular Weight:
NCBI Full Name:Survival of motor neuron-related-splicing factor 30
NCBI Synonym Full Names:survival motor neuron domain containing 1
NCBI Official Symbol:SMNDC1  
NCBI Official Synonym Symbols:SMNR; SPF30; TDRD16C  
NCBI Protein Information:survival of motor neuron-related-splicing factor 30
UniProt Protein Name:Survival of motor neuron-related-splicing factor 30
UniProt Synonym Protein Names:30 kDa splicing factor SMNrp; SMN-related protein; Survival motor neuron domain-containing protein 1
Protein Family:Survival of motor neuron-related-splicing factor
UniProt Gene Name:SMNDC1  
UniProt Entry Name:SPF30_HUMAN
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