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Rabbit Anti-CLEC16A/AP Conjugated antibody (bs-18539R-AP)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-18539R-AP
英文名稱 Rabbit Anti-CLEC16A/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標記的C型凝集素結構域家族16成員A抗體
別    名 Protein CLEC16A; C type lectin domain family 16 member A; CL16A; Gop 1; Gop1; CL16A_HUMAN; KIAA0350; MGC111457.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  免疫學  糖尿病  自然殺傷細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Pig, Cow, )
產品應用 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 118kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CLEC16A
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.
產品介紹 background:
This gene encodes a member of the C-type lectin domain containing family. Single nucleotide polymorphisms in introns of this gene have been associated with diabetes mellitus, multiple sclerosis and rheumatoid arthritis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]

Subcellular Location:
Cell membrane, Cytoplasmic.

Tissue Specificity:
Almost exclusively expressed in immune cells, including dendritic cells, B-lymphocytes and natural killer cells.

DISEASE:
Insulin-dependent diabetes mellitus is significantly associated with variation within a 233-kb linkage disequilibrium block on chromosome 16p13 that includes KIAA0350. Three common non-coding variants of KIAA0350 in strong linkage disequilibrium reach genome-wide significance for association with the disease.

Similarity:
Belongs to the CLEC16A/gop-1 family.

Database links:

Entrez Gene: 23274 Human

Entrez Gene: 74374 Mouse

Omim: 611303 Human

SwissProt: Q2KHT3 Human

SwissProt: Q80U30 Mouse



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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