產(chǎn)品編號(hào) | bs-13785R |
英文名稱 | C19orf48 Rabbit pAb |
中文名稱 | 19號(hào)染色體開(kāi)放閱讀框48抗體 |
別 名 | C19orf48; CS048_HUMAN; Multidrug resistance-related protein; Uncharacterized protein C19orf48; Multidrug resistance-related protein, isoform CRA_a; MGC13170; hCG_2008493; |
研究領(lǐng)域 | 腫瘤 細(xì)胞生物 免疫學(xué) 糖尿病 淋巴細(xì)胞 |
抗體來(lái)源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | (predicted: Human) |
產(chǎn)品應(yīng)用 | IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/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 | 13 kDa |
檢測(cè)分子量 | |
細(xì)胞定位 | 細(xì)胞外基質(zhì) |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human C19orf48: 21-117/117 |
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(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
PubMed | PubMed |
產(chǎn)品介紹 |
Consisting of around 63 million bases with over 1,400 genes, chromosome 19 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. The C19orf48 gene product has been provisionally designated C19orf48 pending further characterization. SWISS: Q6RUI8 Gene ID: 84798 Database links: Entrez Gene: 84798 Human SwissProt: Q6RUI8 Human Unigene: 256301 Human |
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