C1orf112 Antibody ALEXA FLUOR

C1orf112 Antibody ALEXA FLUOR is available 5 times from Bioss primary conjugated antibodies. alexa fluor labs

bs-15008R-A350 | C1orf112 Antibody, ALEXA FLUOR 350size: 100ul | 376.71 USD

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bs-15008R-A488 | C1orf112 Antibody, ALEXA FLUOR 488size: 100ul | 376.71 USD

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bs-15008R-A555 | C1orf112 Antibody, ALEXA FLUOR 555size: 100ul | 376.71 USD

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bs-15008R-A594 | C1orf112 Antibody, ALEXA FLUOR 594size: 100ul | 376.71 USD

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bs-15008R-A647 | C1orf112 Antibody, ALEXA FLUOR 647size: 100ul | 376.71 USD

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  • Category
    Conjugated Primary Antibodies
  • Host Organism
    Rabbit (Oryctolagus cuniculus)
  • Target Antigen
    C1orf112
  • Specificity
    This is a highly specific antibody against C1orf112.
  • Modification
    Unmodified
  • Modification Site
    None
  • Clonality
    Polyclonal
  • Clone
    Polyclonal antibody
  • Concentration
    1ug per 1ul
  • Immunogen range
    250-300/853
  • Subcellular location
    Cytoplasm, Nucleus
  • Source
    This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human C1orf112
  • Gene ID Number
    55732
  • Swiss Prot
    Q9NSG2
  • Tested applications
    IF(IHC-P)
  • Recommended dilutions
    IF(IHC-P)(1:50-200)
  • Crossreactivity
    Human, Mouse, Rat
  • Cross-reactive species details
    Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.
  • Background of the antigen
    Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf112 gene product has been provisionally designated C1orf112 pending further characterization.
  • Purification
    Purified by Protein A.
  • Storage conditions
    Store this antibody in aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide. Keep refrigerated at 2 to 8 degrees Celcius for up to one year.
  • Synonyms
    Uncharacterized protein C1orf112; C1orf112
  • Gene target
  • Short name
    C1orf112 Antibody,
  • Technique
    Antibody
  • Alternative technique
    antibodies
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