Carbonic Anhydrase VIII / Unconjugated / CPTC-CA8-2
Carbonic Anhydrase VIII / Unconjugated / CPTC-CA8-2
Product Details
Supplier | Biotium | |
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Catalog #: | BNUM2232-50 (View supplier product page) | |
Size | 50 μl | |
Price | $410.00 | |
Antigen | Carbonic Anhydrase VIII | |
Clone | CPTC-CA8-2 | |
Host | Mouse | |
Isotype | IgG2a κ | |
Conjugate | Unconjugated | |
Target Species | Human | |
Applications | IHC, IHC-P, WB | |
Description | Carbonic anhydrase VIII (carbonic anhydrase 8) was named because of sequence similarity to other known carbonic anhydrase genes. However, the gene product lacks carbonic anhydrase activity (i. e. , the reversible hydration of carbon dioxide). The gene product continues to carry a carbonic anhydrase designation based on clear sequence identity to other members of the carbonic anhydrase gene family. Mutations in the gene cause neurological disorders in mice. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors. |
About Carbonic Anhydrase VIII and Purified
Carbonic Anhydrase VIII | The protein encoded by this gene was initially named CA-related protein because of sequence similarity to other known carbonic anhydrase genes. However, the gene product lacks carbonic anhydrase activity (i.e., the reversible hydration of carbon dioxide). The gene product continues to carry a carbonic anhydrase designation based on clear sequence identity to other members of the carbonic anhydrase gene family. The absence of CA8 gene transcription in the cerebellum of the lurcher mutant in mice with a neurologic defect suggests an important role for this acatalytic form. Mutations in this gene are associated with cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 (CMARQ3). Polymorphisms in this gene are associated with osteoporosis, and overexpression of this gene in osteosarcoma cells suggests an oncogenic role. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
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$410.00
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