產(chǎn)品編號(hào) | bs-16098R |
英文名稱 | FKSG24 Rabbit pAb |
中文名稱 | MPV17L2蛋白抗體 |
別 名 | FKSG 24; MGC110861; MGC12972; M17L2_HUMAN; MPV17 mitochondrial membrane protein like 2; MPV17L2; Uncharacterized protein FKSG24. |
研究領(lǐng)域 | 細(xì)胞生物 免疫學(xué) |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
克 隆 號(hào) | |
交叉反應(yīng) | (predicted: Human,Mouse,Rat,Pig,Sheep,Cow,Dog,Horse) |
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 | 23 kDa |
檢測分子量 | |
細(xì)胞定位 | 細(xì)胞膜 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human FKSG24: 121-206/206 |
亞 型 | |
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 Fc?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 MPV17L2 gene product has been provisionally designated MPV17L2 pending further characterization. Function: FKSG24 is a potential multi-pass membrane protein. It belongs to the peroxisomal membrane protein PXMP2/4 family. The exact function of FKSG24 remains unknown. Subcellular Location: Membrane; Multi-pass membrane protein (potential) Similarity: Belongs to the peroxisomal membrane protein PXMP2/4 family. SWISS: Q567V2 Gene ID: 84769 Database links: Entrez Gene: 84769 Human Entrez Gene: 234384 Mouse SwissProt: Q567V2 Human SwissProt: Q8VIK2 Mouse |