货号 | AF-396-SP |
别名 | Neuregulin1 beta 1; Neuregulin-1 beta 1 |
反应种属 | Human |
应用 | Western Blot,Immunohistochemistry,Neutralization |
目标/特异性 | Detects human NRG1‑ beta 1/HRG1‑ beta 1 EGF Domain in direct ELISAs and Western blots. In Western blots (reducing conditions), approximately 100% cross‑reactivity with recombinant human HRG-alpha is observed. In direct ELISAs, approximately 5% cross‑reactivity with recombinant human HRG-alpha is observed. |
使用方法 | Western Blot: 0.1 µg/mL Immunohistochemistry: 5-15 µg/mL Neutralization: Measured by its ability to neutralize NRG1‑ beta 1/HRG1‑ beta 1-induced proliferation in the MCF‑7 human breast cancer cell line. Karey, K. P. et al. (1988) Cancer Research 48:4083. The Neutralization Dose (ND50) is typically 0.5‑2.0 µg/mL in the presence of 0.75 ng/mL Recombinant Human NRG1‑ beta 1/HRG1‑ beta 1 EGF Domain. |
来源 | Polyclonal Goat IgG |
产品组分 |
供应商 | R&D Systems |
Entrez Gene IDs | 3084 (Human); 211323 (Mouse); 112400 (Rat) |
应用文献 | |
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions. Preventive effects of heregulin-beta1 on macrophage foam cell formation and atherosclerosis. | |
纯化方式 | Antigen Affinity-purified |
免疫原 | E. coli-derived recombinant human NRG1‑ beta 1/HRG1‑ beta 1 EGF Domain Thr176-Lys246 Accession # NP_039250 |
内毒素水平 | <0.10 EU per 1 μg of the antibody by the LAL method. |
生物活性 | Human |
标记 | Unconjugated |
溶解方法 | Reconstitute at 0.2 mg/mL in sterile PBS. |
背景 | The neuregulin family of structurally related glycoproteins comprises products from four distinct but related genes, Nrg-1, Nrg-2, Nrg-3, and Nrg-4. Through alternative splicing or the use of alternative promoters, Nrg-1 has been shown to encode more than 14 soluble or transmembrane proteins. The extracellular domain of the transmembrane NRG1 isoforms can be proteolytically cleaved to release soluble growth factors. All NRG1 isoforms contain an EGF‑like domain ( alpha - or beta -splice variant that differ in their C-terminal region) that is required for their direct binding to the ErbB3 or ErbB4 receptor tyrosine kinases. The ErbB3 or ErbB4 subsequently recruits and heterodimerizes with ErbB2, resulting in tyrosine phosphorylation and NRG1 signaling. NRG1 isoforms can be classified into three major subtypes. Type I (Neu Differentiation Factor, NDF; Heregulin, HRG; Acetylcholine Receptor Inducing Activity, ARIA) and type II (Glial Growth Factor, GGF) NRG1s have an immunoglobulin (Ig)-like domain N-terminal to the EGF‑like domain. Type I NRG1s differ from type II NRG1s by having a glycosylation-rich domain between the Ig‑like and the EGF‑like domains. Type III NRG1s (Sensory and Motor neuron-Derived Factor) lacks the Ig‑like domain but has a cysteine rich domain (CRD) instead. NRG1 isoforms show distinct spatial and temporal expression patterns. These proteins play important roles during development of both the nervous system and the heart. They have been shown to regulate the selective expression of neurotransmitter receptors in neurons and at the neuromuscular junction, and promote the differentiation and development of Schwann cells from neural crest stem cells. NRG1s have also been shown to be involved in the establishment of the oligodendroglial lineage. |
运输条件 | Blue Ice |
存放说明 | 4℃ |
参考文献 |
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Cell Proliferation Induced by NRG1‑ beta 1/HRG1‑ beta 1 and Neutralization by Human NRG1‑ beta 1/HRG1‑ beta 1 Antibody. Recombinant Human NRG1‑ beta 1/ | |
NRG1‑ beta 1/HRG1‑ beta 1 in Human Breast. NRG1‑ beta 1/HRG1‑ beta 1 was detected in immersion fixed paraffin-embedded sections of human breast using Goat Anti-Human NRG1‑ beta 1/HRG1‑ beta 1 EGF Domain Antigen Affinity-purified Polyclonal Antibody (Catalog # AF-396-NA) at 1 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS008) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections. |