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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 350 size: 100ul | 378.97 USD

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bs-15008R-A488 | C1orf112 Antibody, ALEXA FLUOR 488 size: 100ul | 378.97 USD

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bs-15008R-A555 | C1orf112 Antibody, ALEXA FLUOR 555 size: 100ul | 378.97 USD

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bs-15008R-A594 | C1orf112 Antibody, ALEXA FLUOR 594 size: 100ul | 378.97 USD

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bs-15008R-A647 | C1orf112 Antibody, ALEXA FLUOR 647 size: 100ul | 378.97 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 targetC1orf112
Short name C1orf112 Antibody,
Technique Antibody
Alternative technique antibodies
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