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Rabbit Anti-IGSF22/AP Conjugated antibody (bs-18140R-AP)
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-18140R-AP
英文名稱1 Rabbit Anti-IGSF22/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標(biāo)記的免疫球蛋白超家族成員22抗體
別    名 Immunoglobulin superfamily member 22.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  細(xì)胞膜受體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Dog, Cat, )
產(chǎn)品應(yīng)用 WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 100kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human IGSF22
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 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.
產(chǎn)品介紹 background:
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.

Database links:

Entrez Gene: 283284 Human

SwissProt: Q8N9C0 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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