Human DNA repair protein complementing XP-G cells (ERCC5)

  • Catalog number
    CSB-EP007773HU-1MG
  • Price
    Please ask
  • Size
    1MG
  • Description
    Recombinant Human DNA repair protein complementing XP-G cells(ERCC5),partial expressed in E.coli
  • Specifications
    Uniprot ID: P28715; Host: Homo sapiens (Human); Expression system: E.coli; Expression region: 947-1186aa; Sequence information: Partial; Tag: N-terminal 6xHis-tagged; Purity: Greater than 90% as determined by SDS-PAGE.
  • Additional_information
    MW: 30.8 kDa; Buffer composition: Tris-based buffer with 50% glycerol.
  • Storage_and_shipping
    Shipped on ice packs (+4°C). The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C. Repeated freezing and thawing should be avoided. Store working aliquots at 4°C for up to one week.
  • Notes
    For research use only.
  • 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.
  • Gene target
    DNA   repair   protein   complementing   XP-G   cells   ERCC5  
  • Gene symbol
    BIVM-ERCC5, IGHV3-71, ERCC5, HLA-G, POLH, NCAPG, FOLR3, SNRPG, PRKDC, GNAO1
  • Short name
    DNA repair protein complementing XP-G cells (ERCC5)
  • Technique
    dna
  • Species
    Human, Humans
  • Alternative name
    H. sapiens Desoxyribonucleic acid repair protein complementing XP-G cells (excision repair cross-complementing rodent repair deficiency, complementation family 5)
  • Alternative to gene target
    excision repair cross-complementing rodent repair deficiency, complementation group 5, COFS3 and ERCC5-201 and ERCM2 and UVDR and XPG and XPGC, ERCC5 and IDBG-49163 and ENSG00000134899 and 2073, protein N-terminus binding, nuclei
  • Tissue
    cells
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    immunoglobulin heavy variable 3-71 (pseudogene)
  • Synonyms gene
  • Synonyms gene name
    • immunoglobulin heavy variable 3-71
    • immunoglobulin heavy variable 3-G pseudogene (provisional)
    • immunoglobulin heavy variable 3-G (provisional)
    • immunoglobulin heavy variable 3-71 pseudogene
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    2000-04-04
  • Entrez gene record
  • RefSeq identity
  • Classification
    • Immunoglobulin heavy locus at 14q32.33
  • VEGA ID
Gene info
  • Identity
  • Gene
  • Long gene name
    ERCC excision repair 5, endonuclease
  • Synonyms gene
  • Synonyms gene name
    • xeroderma pigmentosum, complementation group G
    • excision repair cross-complementing rodent repair deficiency, complementation group 5
    • excision repair cross-complementation group 5
  • Synonyms name
  • GenBank acession
  • Locus
  • Discovery year
    2001-06-22
  • Entrez gene record
  • Pubmed identfication
  • Classification
    • Xeroderma pigmentosum complementation groups
    • ERCC excision repair associated
  • VEGA ID
  • Locus Specific Databases
Gene info
Gene info
Gene info
Gene info
Gene info
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    G protein subunit alpha o1
  • Synonyms gene name
    • guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
  • Synonyms
  • Locus
  • Discovery year
    1988-04-24
  • Entrez gene record
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • G protein subunits alpha, group i
    • MicroRNA protein coding host genes
  • VEGA ID
MeSH Data
  • Name
  • Concept
    Scope note: A technique which uses synthetic oligonucleotides to direct the cell's inherent DNA repair system to correct a mutation at a specific site in an episome or chromosome.
  • Tree numbers
    • E02.095.301.500
    • E05.393.420.301.500
    • E05.393.420.601.575.500
  • Qualifiers
    legislation & jurisprudence, ethics, mortality, psychology, trends, veterinary, history, classification, economics, instrumentation, methods, nursing, standards, adverse effects, statistics & numerical data
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