| 产品编号 | bs-6643R |
| 英文名称 | SCYL1BP1 Rabbit pAb |
| 中文名称 | SCYL结合蛋白1抗体 |
| 别 名 | GO; NTKLBP1; SCYL1BP1; NTKL-BP1; SCYL1-BP1; GORAB_HUMAN; GORAB; N-terminal kinase-like-binding protein 1 (NTKL-BP1 | NTKL-binding protein 1 | hNTKL-BP1); SCY1-like 1-binding protein 1 (SCYL1-BP1 | SCYL1-binding protein 1); GORAB_MOUSE; N-terminal kinase-like-binding protein 1 (NTKL-BP1 | NTKL-binding protein 1 | mNTKL-BP1); GORAB_RAT; N-terminal kinase-like-binding protein 1 (NTKL-BP1 | NTKL-binding protein 1); golgin, RAB6 interacting; SCY1-like 1 binding protein 1; golgin, RAB6-interacting; gerodermia osteodysplastica; RAB6-interacting golgin |
| 研究领域 | 细胞生物 信号转导 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, (predicted: Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, ) |
| 产品应用 | WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复）
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理论分子量 | 45kDa |
| 检测分子量 | 55 |
| 细胞定位 | 细胞浆 |
| 性 状 | Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human SCYL1BP1: 201-300/394 |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 缓 冲 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 保存条件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| PubMed | PubMed |
| 产品介绍 |
Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070]; also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation. Subunit: Interacts with SCYL1 (By similarity). Interacts with RCHY1 and RAB6A/RAB6. Subcellular Location: Cytoplasm. Golgi apparatus. DISEASE: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070]; also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation. Similarity: Belongs to the GORAB family. SWISS: Q5T7V8 Gene ID: 92344 Database links: Entrez Gene: 92344 Human Entrez Gene: 98376 Mouse Omim: 607983 Human SwissProt: Q5T7V8 Human SwissProt: Q8BRM2 Mouse Unigene: 183702 Human Unigene: 32901 Mouse Unigene: 45710 Rat |
| 产品图片 |
Sample: HepG2 Cell (Human) Lysate at 40 ug
Primary: Anti-SCYL1BP1 (bs-6643R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 45 kD
Observed band size: 55 kD
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| 1、抗体溶解方法 | |
| 2、抗体修复方式 | |
| 3、常用试剂的配制 | |
| 4、免疫组化操作步骤 | |
| 5、免疫组化问题解答 | |
| 6、Western Blotting 操作步骤 | |
| 7、Western Blotting 问题解答 | |
| 8、关于肽链的设计 | |
| 9、多肽的溶解与保存 | |
| 10、酶标抗体效价测定程序 | |
