Application
ATOH8 Antibody (N-term) western blot analysis in human normal Uterus tissue lysates (35ug/lane).This demonstrates the ATOH8 antibody detected the ATOH8 protein (arrow).Application
ATOH8 Antibody (N-term) western blot analysis in mouse liver tissue lysates (35ug/lane).This demonstrates the ATOH8 antibody detected the ATOH8 protein (arrow).| Product Name | ATOH8 Antibody (N-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WB |
| WB:1:100~500 |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | ATH6, BHLHA21 |
|---|---|
| Alternative Names | ATOH8 ATH6 BHLHA21 Protein atonal homolog 8 Class A basic helix-loop-helix protein 21 Helix-loop-helix protein hATH-6 |
| Molecular Weight(MW) | 34644 Da |
| Function | Putative transcription factor. May be implicated in specification and differentiation of neuronal cell lineages in the brain. May participate in kidney development and may be involved in podocyte differentiation (By similarity) |
| Tissue Specificity | Expressed in lung, liver, kidney, heart and pancreas. Expressed in endothel of umbilical vessels |
| Cellular Localization | Nucleus (By similarity). |
| Entrez Gene | 84913 |
|---|---|
| Nucleotide Accession | NP_116216.2 |
Application
ATOH8 Antibody (N-term) western blot analysis in human normal Uterus tissue lysates (35ug/lane).This demonstrates the ATOH8 antibody detected the ATOH8 protein (arrow).
Application
ATOH8 Antibody (N-term) western blot analysis in mouse liver tissue lysates (35ug/lane).This demonstrates the ATOH8 antibody detected the ATOH8 protein (arrow).| Application Notes | WB:1:100~500 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
