C19orf42,19号染色体开放阅读框42抗体

产品编号HZ-13783R
英文名称C19orf42
中文名称19号染色体开放阅读框42抗体
别 名C19orf42; Chromosome 19 open reading frame 42; CS042_HUMAN; MGC2747; UPF0608 protein C19orf42; UPF0608 protein C19orf42 homolog.
说 明 书0.1ml 0.2ml
研究领域细胞生物 神经生物学 信号转导 淋巴细胞
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat, Cow,
C19orf42,19号染色体开放阅读框42抗体产品应用WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 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7kDa
细胞定位细胞膜
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C19orf42
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.
C19orf42,19号染色体开放阅读框42抗体PubMedPubMed
产品介绍background:
C19orf42 (chromosome 19 open reading frame 42) is a 75 amino acid single-pass type I membrane 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.

Subcellular Location:
Membrane.

Similarity:
Belongs to the UPF0608 family.

Gene ID:
79086

Database links:
Entrez Gene: 79086 Human
SwissProt: Q9BQ49 Human
Unigene: 356467 Human

C19orf42,19号染色体开放阅读框42抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.