货号 | AF5739-SP |
别名 | CRP; CRP1; CSRPCYRP; CYRP; cysteine and glycine-rich protein 1; Cysteine-rich protein 1; D1S181E; DKFZp686M148; LIM-domain protein | 全称 | Cysteine-rich Protein 1 |
反应种属 | Human/Mouse/Rat |
应用 | Western Blot(0.5 µg/mL) |
目标/特异性 | Detects human, mouse, and rat CSRP1 in Western blots. |
使用方法 | Western Blot: 0.5 µg/mL |
来源 | Reconstitute at 0.2 mg/mL in sterile PBS. |
产品组分 |
供应商 | R&D Systems |
Entrez Gene IDs | 1465 (Human); 13007 (Mouse); 29276 (Rat) |
纯化方式 | Antigen Affinity-purified |
免疫原 | E. coli-derived recombinant human CSRP1 Met1-Glu193 Accession # P21291 |
生物活性 | Human, Mouse, Rat |
标记 | Unconjugated |
溶解方法 | Reconstitute at 0.2 mg/mL in sterile PBS. |
背景 | CSRP1 (Cysteine-rich protein 1; also CRP1 and Cysteine and Glycine‑rich protein 1) is a 23 kDa cytoplasmic member of the CRP family of LIM domain‑containing proteins. It is expressed in both visceral and vascular smooth muscle, and interacts with zyxin and alpha ‑actinin, two proteins involved in actin assembly and crosslinking, during muscle cell differentiation. Human CSRP1 is 193 amino acids (aa) in length and contains two 50 aa LIM (for lin11/isl1/mec3) domains that contain two zinc‑finger motifs (aa 10‑61 and 119‑171), an NLS between aa 64‑69, and a Gly-rich C-terminus (aa 176‑187). There are two likely phosphorylation sites at Tyr127 and Ser192. Full‑length human CSRP1 shares 99% aa identity with mouse CSRP1. |
运输条件 | Blue Ice |
存放说明 | 4℃ |
Detection of Human, Mouse, and Rat CSRP1 by Western Blot. Western blot shows lysates of ME-180 human cervical epithelial carcinoma cell line, HT-2 mouse T cell line, and Rat-2 rat embryonic fibroblast cell line. PVDF membrane was probed with 0.5 µg/mL Goat Anti-Human/Mouse/Rat CSRP1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5739) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF109). For additional reference, recombinant human CSRP1, CSRP2, CSRP3 (5 ng/lane) were included. A specific band for CSRP1 was detected at approximately 23 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1. |