SMN1 Antibody, Cy3 Conjugated

• Catalog number
  bs-4628R-Cy3
• Price
  Please ask
• Size
  0.1ml

• Long name
  SMN1 Polyclonal Antibody, Cy3 Conjugated
• Category
  Conjugated Primary Antibodies
• Conjugation
  Cy3
• Host Organism
  Rabbit (Oryctolagus cuniculus)
• Target Antigen
  SMN1
• Specificity
  This is a highly specific antibody against SMN1. 100% sequence similarity to SMN-delta7, SMN-delta5, SMN-delta57
• Modification
  Unmodified
• Modification site
  None
• Clonality
  Polyclonal
• Clone
  Polyclonal antibody
• Concentration
  1ug per 1ul
• Immunogen_range
  60-95/294
• Source
  KLH conjugated synthetic peptide derived from human SMN1
• Gene ID number
  6606
• Tested applications
  IF(IHC-P)
• Recommended dilutions
  IF(IHC-P)(1:50-200)
• Crossreactivity
  Human, Mouse, Rat
• Crossreactive species details
  Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.
• Antigen background
  SMN1 is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. While mutations in the telomeric copy are associated with spinal muscular atrophy, mutations in this gene, the centromeric copy, do not lead to disease. This gene may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Four transcript variants encoding distinct isoforms have been described.
• Purification method
  This antibody was purified via Protein A.
• Storage conditions
  Keep the antibody in an aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide. Store refrigerated at 2 to 8 degrees Celcius for up to 1 year.
• Excitation Emission
  512,550nm/570,615nm
• Synonyms
  Component of gems 1; Component of gems 2; Gemin 1; Gemin-1; SMA; SMA1; SMA3; SMN; SMN_HUMAN; SMN1; SMN2; SMNC; SMNT; Survival motor neuron protein; survival of motor neuron 1, telomeric; survival of motor neuron 2, centromeric.
• Properties
  If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies they should be stored frozen at - 24°C for long term storage and for short term at + 5°C. Cy3 antibodies are excited by the 488-nanometer wave of an argon laser and the 633-nanometer line of a helium-neon diode laser. 1 of the Anti-SMN1 can be used in flow cytometry but typically shows lower fluorescence intensity comparable to that of PE or APC. This Bioss Primary Conjugated Antibodies antibody is well suited for fluorescent microscopy.
• Additional conjugation
  cy3 conjugation kit
• French translation
  anticorps

• Gene target
  SMN1   Conjugated  
• Gene symbol
  SMN1
• Short name
  Anti-SMN1
• Technique
  Antibody, antibodies against human proteins, antibodies for, antibody Conjugates
• Isotype
  Immunoglobulin G (IgG)
• Label
  Cy3
• Alternative name
  Anti-SMN1 PAb Cy3
• Alternative technique
  antibodies

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
  Blotting, Western
• Concept
  Scope note: Identification of proteins or peptides that have been electrophoretically separated by blot transferring from the electrophoresis gel to strips of nitrocellulose paper, followed by labeling with antibody probes.
• Tree numbers
  • E05.196.401.143
  • E05.301.300.096
  • E05.478.566.320.200
  • E05.601.262
  • E05.601.470.320.200
• Qualifiers
  ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data

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