Recombinant Human Survival Motor Neuron Domain Containing 1

• Catalog number
  7-06422
• Price
  Please ask
• Size
  10µg

• Shelf life
  The shelf life of this product is 12 mois
• Storage
  The storage of this product is at: -20℃
• Shipping
  The shipping of this product is in: RT
• Properties
  Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.
• Source
  Recombinants or rec. proteins
• Group
  recombinants

• Gene target
  Survival   Motor   Neuron   Domain  
• Gene symbol
  SMNDC1, SMN1
• Short name
  Recombinant Survival Motor Neuron Domain 1
• Technique
  Recombinant, E. coli recombinant proteins are genetic recombinations in Escherichia coli, supplied as white sterile powder lyopillized. CHI Scientific advises they will be reconstituted in a buffer soluion or culture medium for cell culture.
• Species
  Human, Humans
• Alternative name
  Rec. H. sapiens Survival Motor Neuron Domain Containing 1
• Alternative technique
  rec

Gene info

• Identity
  HGNC:16900
• Gene
  SMNDC1
• Long gene name
  survival motor neuron domain containing 1
• Synonyms
  • SPF30
  • SMNR
  • TDRD16C
• Synonyms name
  • splicing factor 30, survival of motor neuron-related
  • tudor domain containing 16C
• GenBank acession
  • AF083385
• Locus
  10q25.2
• Discovery year
  2003-11-06
• Entrez gene record
  10285
• Pubmed identfication
  • 9731529
  • 9817934
• RefSeq identity
  • NM_005871
• Classification
  • Tudor domain containing
  • Spliceosomal A complex
• VEGA ID
  OTTHUMG00000019036

Gene info

• Identity
  HGNC:11117
• Gene
  SMN1
• Long gene name
  survival of motor neuron 1, telomeric
• Synonyms gene
  • SMA@
  • SMA
• Synonyms gene name
  • spinal muscular atrophy (Werdnig-Hoffmann disease, Kugelberg-Welander disease)
• Synonyms
  • BCD541
  • SMNT
  • SMA1
  • SMA2
  • SMA3
  • GEMIN1
  • TDRD16A
• Synonyms name
  • gemin-1
  • tudor domain containing 16A
• GenBank acession
  • U18423
• Locus
  5q13.2
• Discovery year
  1996-12-12
• Entrez gene record
  6606
• Pubmed identfication
  • 7813012
• RefSeq identity
  • NM_000344
• Classification
  • SMN complex
  • Tudor domain containing
• VEGA ID
  OTTHUMG00000099361
• Locus Specific Databases
  • SMN1 - Spinal Muscular Atrophy (SMA)
  • Leiden Muscular Dystrophy pages
  • ALSOD, the Amyotrophic Lateral Sclerosis Online Genetic Database
  • LRG_676

MeSH Data

• Name
  Primary Cell Culture
• Concept
  Scope note: The initial culturing of cells derived directly from fresh TISSUES.
• Tree numbers
  • E01.370.225.500.223.500
  • E05.200.500.265.500
  • E05.242.223.500
  • E05.481.500.249.500
• Qualifiers
  ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data

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