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KK-LC-1/CT83 Rabbit pAb (bs-16747R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-16747R
英文名稱 KK-LC-1/CT83 Rabbit pAb
中文名稱 癌/睪丸抗原83抗體
別    名 Cancer/testis antigen 83; Chromosome X open reading frame 61; CT83; CXorf61; Kita-kyushu lung cancer antigen 1; KK-LC-1; KKLC1; KKLC1_HUMAN.  
研究領域 腫瘤  細胞生物  免疫學  腫瘤細胞生物標志物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human)
產品應用 IHC-P=1:100-500,IHC-F=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 13 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KK-LC-1/CT83: 51-113/113 <Extracellular>
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 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The KK-LC-1 gene product has been provisionally designated KK-LC-1 pending further characterization.

Function:
Specifically expressed in testis. Expressed by cancer cell lines.

Subcellular Location:
Cell membrane.

SWISS:
Q5H943

Gene ID:
203413

Database links:

Entrez Gene: 203413 Human

SwissProt: Q5H943 Human

Unigene: 97892 Human



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