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Rabbit Anti-C19orf56  antibody (bs-20046R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-20046R
英文名稱 Rabbit Anti-C19orf56  antibody
中文名稱 19號染色體開放閱讀框56抗體
別    名 C19orf56; Chromosome 19 open reading frame 56; ASTER_HUMAN; Hypothetical protein LOC51398; PTD008; UPF0139 membrane protein C19orf56.  
研究領域 腫瘤  細胞生物  糖尿病  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Pig,Sheep,Cow)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 12kDa
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C19orf56: 31-106/106 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 C19orf56 is a 106 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.

Subcellular Location:
Membrane.

Similarity:
Belongs to the UPF0139 (CGI-140) family.

SWISS:
Q9Y284

Gene ID:
51398

Database links:

Entrez Gene: 51398 Human

SwissProt: Q9Y284 Human

SwissProt: Q6ZWX0 Mouse

Unigene: 108969 Human

Unigene: 657204 Human



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