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Rabbit Anti-SBK2/BF647 Conjugated antibody (bs-17250R-BF647)
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-17250R-BF647
英文名稱 Rabbit Anti-SBK2/BF647 Conjugated antibody
中文名稱 BF647標記的絲氨酸/蘇氨酸蛋白激酶SBK2抗體
別    名 Sbk2; SBK2_HUMAN; Serine/threonine-protein kinase SBK2; SgK069; SH3-binding domain kinase family member 2; Sugen kinase 69.  
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  信號轉導  激酶和磷酸酶  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, )
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 38kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SBK2
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 癈 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癈. 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 癈.
產品介紹 background:
SBK2 is a 348 amino acid protein that belongs to the protein kinase superfamily, the Ser/Thr protein kinase family and the STKL subfamily. SBK2 contains one protein kinase domain. The SBK2 gene is conserved in chimpanzee, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 19q13.42. Chromosome 19 consists of approximately 63 million bases and 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.

Subcellular Location:
cytoplasm

Similarity:
Belongs to the protein kinase superfamily.
Ser/Thr protein kinase family. STKL subfamily.
Contains 1 protein kinase domain.

Database links:

Entrez Gene: 646643 Human

SwissProt: P0C263 Human

Unigene: 532676 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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