FITC Anti-Mouse TER-119 (TER-119)
The TER-119 antibody is named for the antigen to which it binds, a 52 kDa surface protein that is associated with glycophorin-A. TER-119 is considered to be a lineage marker for later stages of erythroid cell development, as its expression begins at the pro-erythroblast stage. TER-119 antigen is not expressed at either BFU-E or CFU-E stages, i.e. prior to the pro-erythroblast stage.
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Recent Publications:
Itokazu M, Onodera Y, Mori T, Inoue S, Yamagishi K, Moritake A, Iwawaki N, Shigi K, Takehara T, Higashimoto Y, Akagi M, Teramura T. Adipose-derived exosomes block muscular stem cell proliferation in aged mouse by delivering miRNA Let-7d-3p that targets transcription factor HMGA2. J Biol Chem. 2022 Jun 6:102098. doi: 10.1016/j.jbc.2022.102098. Epub ahead of print. PMID: 35679898.
Baba T, Yoshida T, Tanabe Y, et al. Cytoplasmic DNA accumulation preferentially triggers cell death of myeloid leukemia cells by interacting with intracellular DNA sensing pathway. Cell Death Dis. 2021 Mar 26;12(4):322. doi: 10.1038/s41419-021-03587-x. PMID: 33771977. Â
| Name | FITC Anti-Mouse TER-119 (TER-119) |
|---|---|
| Cat. No. | 35-5921 |
| Alternative Names | TER119, Erythroid cell marker, Ly-76, Ly76 |
| Gene ID | 104231 |
| Clone | TER-119 |
| Isotype | Rat IgG2b, κ |
| Reactivity | Mouse |
| Format | FITC |
| Application | Flow Cytometry |
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FITC Anti-Mouse TER-119 (TER-119)
The TER-119 antibody is named for the antigen to which it binds, a 52 kDa surface protein that is associated with glycophorin-A. TER-119 is considered to be a lineage marker for later stages of erythroid cell development, as its expression begins at the pro-erythroblast stage. TER-119 antigen is not expressed at either BFU-E or CFU-E stages, i.e. prior to the pro-erythroblast stage.
Â
Recent Publications:
Itokazu M, Onodera Y, Mori T, Inoue S, Yamagishi K, Moritake A, Iwawaki N, Shigi K, Takehara T, Higashimoto Y, Akagi M, Teramura T. Adipose-derived exosomes block muscular stem cell proliferation in aged mouse by delivering miRNA Let-7d-3p that targets transcription factor HMGA2. J Biol Chem. 2022 Jun 6:102098. doi: 10.1016/j.jbc.2022.102098. Epub ahead of print. PMID: 35679898.
Baba T, Yoshida T, Tanabe Y, et al. Cytoplasmic DNA accumulation preferentially triggers cell death of myeloid leukemia cells by interacting with intracellular DNA sensing pathway. Cell Death Dis. 2021 Mar 26;12(4):322. doi: 10.1038/s41419-021-03587-x. PMID: 33771977. Â
| Name | FITC Anti-Mouse TER-119 (TER-119) |
|---|---|
| Cat. No. | 35-5921 |
| Alternative Names | TER119, Erythroid cell marker, Ly-76, Ly76 |
| Gene ID | 104231 |
| Clone | TER-119 |
| Isotype | Rat IgG2b, κ |
| Reactivity | Mouse |
| Format | FITC |
| Application | Flow Cytometry |
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Description
The TER-119 antibody is named for the antigen to which it binds, a 52 kDa surface protein that is associated with glycophorin-A. TER-119 is considered to be a lineage marker for later stages of erythroid cell development, as its expression begins at the pro-erythroblast stage. TER-119 antigen is not expressed at either BFU-E or CFU-E stages, i.e. prior to the pro-erythroblast stage.
Â
Recent Publications:
Itokazu M, Onodera Y, Mori T, Inoue S, Yamagishi K, Moritake A, Iwawaki N, Shigi K, Takehara T, Higashimoto Y, Akagi M, Teramura T. Adipose-derived exosomes block muscular stem cell proliferation in aged mouse by delivering miRNA Let-7d-3p that targets transcription factor HMGA2. J Biol Chem. 2022 Jun 6:102098. doi: 10.1016/j.jbc.2022.102098. Epub ahead of print. PMID: 35679898.
Baba T, Yoshida T, Tanabe Y, et al. Cytoplasmic DNA accumulation preferentially triggers cell death of myeloid leukemia cells by interacting with intracellular DNA sensing pathway. Cell Death Dis. 2021 Mar 26;12(4):322. doi: 10.1038/s41419-021-03587-x. PMID: 33771977. Â
| Name | FITC Anti-Mouse TER-119 (TER-119) |
|---|---|
| Cat. No. | 35-5921 |
| Alternative Names | TER119, Erythroid cell marker, Ly-76, Ly76 |
| Gene ID | 104231 |
| Clone | TER-119 |
| Isotype | Rat IgG2b, κ |
| Reactivity | Mouse |
| Format | FITC |
| Application | Flow Cytometry |
