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Description
TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22; mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.
Specifications
Specifications
| Antigen | SR140 |
| Applications | Western Blot, Immunofluorescence, Immunocytochemistry, Immunohistochemistry (Paraffin) |
| Classification | Polyclonal |
| Concentration | 0.44 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 |
| Gene | U2SURP |
| Gene Accession No. | O15042, Q6NV83 |
| Gene Alias | KIAA0332, SR140, U2 associated protein SR140, U2 associated SR140 protein, U2SURP |
| Gene Symbols | U2surp |
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Product Title
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