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Full name | EMC7 rabbit polyclonal antibody |
Alternative names | 50 μl/100 μl |
Reactivity | rabbit polyclonal |
Applications | WB, IHC |
Host | Rabbit |
Clone type | rabbit polyclonal |
Target Background | EMC7, also known as C15orf24, which encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf24 gene product has been provisionally designated C15orf24 pending further characterization. |
Swissprot No | Q9NPA0 |
Gene Accession | NP_064539 |
WB Predicted band size | Immunohistochemical analysis of paraffin-embedded Human breast cancer tissue or EMC7 antigen-treated (Neutralization experiment) using P107475(EMC7 Antibody) at dilution 1/35 |
WB Positive control | P107475-WB-1-P |
WB Recommended dilution | 26 kDa |
IHC predicted cell location | Predicted cell location: Cytoplasm |
IHC positive control | Positive control: Human liver cancer |
IHC Recommed dilution | Recommended dilution: 25-100 |
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
P107475-WB-1-P
Immunohistochemical analysis of paraffin-embedded Human liver cancer tissue or EMC7 antigen-treated (Neutralization experiment) using P107475(EMC7 Antibody) at dilution 1/35
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