SLC35C1
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Official Full Name
solute carrier family 35, member C1 -
Synonyms
fuct1;E430007K15Rik
| Cat.# | Product name | Source (Host) | Species | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| SLC35C1-1888Z | Recombinant Zebrafish SLC35C1 | Mammalian Cell | Zebrafish | His |
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| SLC35C1-4275R | Recombinant Rhesus monkey SLC35C1 Protein, His-tagged | Mammalian Cell | Rhesus macaque | His |
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| SLC35C1-4443C | Recombinant Chicken SLC35C1 | Mammalian Cell | Chicken | His |
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| SLC35C1-4091R | Recombinant Rhesus Macaque SLC35C1 Protein, His (Fc)-Avi-tagged | HEK293 | Rhesus macaque | His&Fc&Avi |
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| SLC35C1-4091R-B | Recombinant Rhesus Macaque SLC35C1 Protein Pre-coupled Magnetic Beads | HEK293 | Rhesus macaque |
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Involved Pathway
SLC35C1 involved in several pathways and played different roles in them. We selected most pathways SLC35C1 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with SLC35C1 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
SLC35C1 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by SLC35C1 itself. We selected most functions SLC35C1 had, and list some proteins which have the same functions with SLC35C1. You can find most of the proteins on our site.
| Function | Related Protein |
|---|
Interacting Protein
SLC35C1 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 SLC35C1 here. Most of them are supplied by our site. Hope this information will be useful for your research of SLC35C1.
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References
- Feng, L; Jiang, H; et al. Negative feedback regulation of Wnt signaling via N-linked fucosylation in zebrafish. DEVELOPMENTAL BIOLOGY 395:268-286(2014).
- Dauber, A; Ercan, A; et al. Congenital disorder of fucosylation type 2c (LADII) presenting with short stature and developmental delay with minimal adhesion defect. HUMAN MOLECULAR GENETICS 23:2880-2887(2014).
