AF251705
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Official Full Name
cDNA sequence AF251705
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Synonyms
AF251705; cDNA sequence AF251705; CLM4; DIgR1; Igsf7; Lmir2; Cd300c; Cd300d; MAIR-II; CMRF35-like molecule; CLM; MAIR-2; Cd300C antigen; Cd300D antigen; leukocyte mono-Ig-like receptor 2; immunoglobulin superfamily member 7; immunoglobulin superfamily, me;
| Species | Cat.# | Product name | Source (Host) | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| Mouse | AF251705-457M | Active Recombinant Mouse AF251705, Fc Chimera | CHO | Fc Chimera |
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| Mouse | AF251705-534M | Active Recombinant Mouse cDNA sequence AF251705, Fc-tagged | CHO | Fc |
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- Involved Pathway
- Protein Function
- Interacting Protein
AF251705 involved in several pathways and played different roles in them. We selected most pathways AF251705 participated on our site, such as Adaptive Immune System, Immune System, Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell, which may be useful for your reference. Also, other proteins which involved in the same pathway with AF251705 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|---|
| Adaptive Immune System | TRAF7;KLC3;UBR2;RNF14;UBE2V2;DZIP3;KLRF1;MALT1;MICA |
| Immune System | AGER;KLHL20;TRIM46;ABI1;TRIM48;RIPK3;RNF14;USP18;BST2 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | CD160;CD200R1;CD200R3;LILRA2;LILRA1;CLEC2H;CD300A;SH2D1B;RAET1E |
AF251705 has several biochemical functions, for example, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by AF251705 itself. We selected most functions AF251705 had, and list some proteins which have the same functions with AF251705. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| protein binding | ENSA;SUMO3;BCKDHB;CTBP1;ANKRD17;TDRD7;TAF11;DOCK10;INHA |
AF251705 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 AF251705 here. Most of them are supplied by our site. Hope this information will be useful for your research of AF251705.
- Q&As
- Reviews
Q&As (10)
Ask a questionGenetic variations or mutations in the gene associated with AF251705 protein may impact its expression or function, potentially affecting cellular processes or disease susceptibility.
AF251705 protein may contribute to disease development or pathophysiological conditions, and the underlying molecular mechanisms are currently being investigated.
The subcellular localization of AF251705 protein can be determined experimentally using techniques such as immunofluorescence microscopy or subcellular fractionation.
Various experimental techniques or assays have been used to study the functional significance of AF251705 protein, including functional genomics approaches, protein-protein interaction studies, or cellular assays.
Dysregulation or dysfunction of AF251705 protein can disrupt cellular homeostasis, perturb molecular signaling networks, and contribute to disease progression.
AF251705 protein may interact with specific molecules or participate in protein complexes, influencing various cellular functions and processes.
The role of AF251705 protein in cellular processes can be investigated experimentally using functional assays or loss-of-function/gain-of-function studies.
Post-translational modifications and regulatory mechanisms may modulate the activity or stability of AF251705 protein.
The expression of AF251705 protein is regulated, and there may be specific factors or signaling pathways involved in its expression control.
AF251705 protein holds the potential to be targeted or manipulated to modulate cellular processes or serve as a potential therapeutic target, warranting further investigation for its therapeutic applications.
Customer Reviews (3)
Write a reviewElucidating protein-protein interactions in protein folding and misfolding diseases.
Deciphering protein-protein interactions in metabolic disorders for therapeutic interventions.
Exploring protein-protein interactions in cell cycle regulation for understanding cell division.
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