產(chǎn)品編號(hào) | bs-18140R |
英文名稱 | Rabbit Anti-IGSF22 antibody |
中文名稱 | 免疫球蛋白超家族成員22抗體 |
別 名 | Immunoglobulin superfamily member 22. |
研究領(lǐng)域 | 細(xì)胞生物 免疫學(xué) 細(xì)胞膜受體 |
抗體來(lái)源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | (predicted: Human,Dog,Cat) |
產(chǎn)品應(yīng)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 | 100kDa |
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 IGSF22: 221-320/903 |
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 |
IGSF22 (immunoglobulin superfamily member 22) is a 903 amino acid protein that contains two fibronectin type-III domains and four Ig-like (immunoglobulin-like) domains, and is a member of the immunoglobulin superfamily. Members of this family of proteins usually localize to the cell membrane, and may act as receptors in immune response pathways. The gene encoding IGSF22 maps to human chromosome 11p15.1. Chromosome 11 houses over 1,400 genes, comprises nearly 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes. Similarity: Contains 2 fibronectin type-III domains. Contains 4 Ig-like (immunoglobulin-like) domains. SWISS: Q8N9C0 Gene ID: 283284 Database links: Entrez Gene: 283284 Human SwissProt: Q8N9C0 Human |