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Full name | CHCHD5 rabbit polyclonal antibody |
Alternative names | 50 μl/100 μl |
Reactivity | rabbit polyclonal |
Applications | WB, IHC |
Host | Rabbit |
Clone type | rabbit polyclonal |
Target Background | CHCHD5 (Coiled-coil-helix-coiled-coil-helix domain-containing protein 5) is a 110 amino acid protein that contains one CHCH domain. The gene encoding CHCHD5 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alström syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. |
Swissprot No | Q9BSY4 |
Gene Accession | BC004498 |
WB Predicted band size | Immunohistochemical analysis of paraffin-embedded Human liver cancer tissue or CHCHD5 antigen-treated (Neutralization experiment) using P109329(CHCHD5 Antibody) at dilution 1/20 |
WB Positive control | P109329-WB-1-P |
WB Recommended dilution | 12 kDa |
IHC predicted cell location | Predicted cell location: Cytoplasm |
IHC positive control | Positive control: Human gastric cancer |
IHC Recommed dilution | Recommended dilution: 20-100 |
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
P109329-WB-1-P
Immunohistochemical analysis of paraffin-embedded Human gastric cancer tissue or CHCHD5 antigen-treated (Neutralization experiment) using P109329(CHCHD5 Antibody) at dilution 1/20
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