C19orf45,19号染色体开放阅读框45抗体-抗体-抗体-生物在线
C19orf45,19号染色体开放阅读框45抗体

C19orf45,19号染色体开放阅读框45抗体

商家询价

产品名称: C19orf45,19号染色体开放阅读框45抗体

英文名称: Anti-C19orf45 antibody

产品编号: HZ-9681R

产品价格: null

产品产地: 中国/美国

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: WB,ELISA,IHC-P,IHC-F,IF

上海沪震实业有限公司
  • 联系人 : 鲍丽雯
  • 地址 : 上海市闵行区闵北路88弄1-30号第22幢AQ136室
  • 邮编 : 200612
  • 所在区域 : 上海
  • 电话 : 139****0749
  • 传真 : 021-60345367
  • 邮箱 : www.shzbio.net

C19orf45,19号染色体开放阅读框45抗体

产品编号HZ-9681R
英文名称C19orf45
中文名称19号染色体开放阅读框45抗体
别 名chromosome 19 open reading frame 45; C19orf45; CS045_HUMAN; FLJ35784; FLJ56642; hypothetical protein LOC374877; Uncharacterized protein C19orf45.
说 明 书0.1ml 0.2ml
研究领域心血管 细胞生物 免疫学 糖尿病
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat,
C19orf45,19号染色体开放阅读框45抗体产品应用WB=1:100-500 ELISA=1:500-1000 IHC-F=1:100-500 ICC=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.
分 子 量57kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C19orf45
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.
C19orf45,19号染色体开放阅读框45抗体PubMedPubMed
产品介绍background:
C19orf45 is a 505 amino acid protein that is 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.

DISEASE:


Similarity:


Database links:
Entrez Gene: 374877 Human
SwissProt: Q8NA69 Human
Unigene: 631862 Human


C19orf45,19号染色体开放阅读框45抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.