C3ORF58
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Official Full Name
chromosome 3 open reading frame 58 -
Synonyms
C3ORF58;chromosome 3 open reading frame 58;UPF0672 protein C3orf58;MGC33365;DIA1;Golgi protein GoPro49
| Cat.# | Product name | Source (Host) | Species | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| C3orf58-0042H | Recombinant Human C3orf58 Protein, GST-Tagged | Wheat Germ | Human | GST |
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| C3orf58-1825H | Recombinant Human C3orf58 Protein, His-tagged | E.coli | Human | His |
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| C3orf58-2603HF | Recombinant Full Length Human C3orf58 Protein, GST-tagged | In Vitro Cell Free System | Human | GST | Full L. 430 amino acids |
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Involved Pathway
C3ORF58 involved in several pathways and played different roles in them. We selected most pathways C3ORF58 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with C3ORF58 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
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Protein Function
C3ORF58 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by C3ORF58 itself. We selected most functions C3ORF58 had, and list some proteins which have the same functions with C3ORF58. You can find most of the proteins on our site.
| Function | Related Protein |
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Interacting Protein
C3ORF58 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with C3ORF58 here. Most of them are supplied by our site. Hope this information will be useful for your research of C3ORF58.
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References
- van Blitterswijk, M; Dejesus-Hernandez, M; et al. Association between repeat sizes and clinical and pathological characteristics in carriers of C90RF72 repeat expansions (Xpansize-72): a cross-sectional cohort study. LANCET NEUROLOGY 12:978-988(2013).
- Thi, HTT; Zhang, ZJ; et al. Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28. JOURNAL OF HUMAN GENETICS 58:33-39(2013).
