FITC标记的19号染色体开放阅读框47抗体
产品名称： FITC标记的19号染色体开放阅读框47抗体
英文名称： Anti-C19orf47/FITC
产品编号： HZ-9683R-FITC
产品价格： null
产品产地： 中国/上海
品牌商标： HZbscience
更新时间： 2023-08-17T10:24:20
使用范围： ICC=1:50-200 IF=1:50-200
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Rabbit Anti-C19orf47/FITC Conjugated antibody
FITC标记的19号染色体开放阅读框47抗体
| 产品编号 | bs-9683R-FITC |
| 英文名称 | Anti-C19orf47/FITC |
| 中文名称 | FITC标记的19号染色体开放阅读框47抗体 |
| 别 名 | Uncharacterized protein C19orf47; Chromosome 19 open reading frame 47; DKFZp686P05129; FLJ36888; Hypothetical protein LOC126526; CS047_HUMAN. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 细胞生物 免疫学 神经生物学 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, |
| 产品应用 | ICC=1:50-200 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 45kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human C19orf47 |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| 产品介绍 | background: C19orf47 is a 422 amino acid protein that exists as three alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. Database links: Entrez Gene: 284325 Human SwissProt: Q5BKX5 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
C19ORF47是一种422个氨基酸的蛋白质，以三个交替剪接的亚型存在，并由位于人类染色体19上的基因编码。第19染色体由大约6300万个碱基组成，占人类基因组DNA的2%以上。第19染色体包括多种有趣的基因，并被公认为具有人类染色体最大的基因密度。它是许多免疫球蛋白超家族成员的遗传宿主，包括杀伤细胞和白细胞Ig样受体、多个ICAMs、CEACAM和PSG家族和Fcα受体。眼睛颜色和头发颜色的关键基因也映射到19号染色体上。Putz JeHHER综合征、脊髓小脑共济失调6型、卒中障碍CADASIL、高胆固醇血症和胰岛素依赖型糖尿病与19号染色体有关。19号染色体和14号染色体易位在某些淋巴增生性疾病中可见，并且通常涉及原癌基因BCL3。