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Rabbit Anti-FAM46A/Cy7 Conjugated antibody (bs-14995R-Cy7)
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-14995R-Cy7
英文名稱1 Rabbit Anti-FAM46A/Cy7 Conjugated antibody
中文名稱 Cy7標記的FAM46A蛋白抗體
別    名 C6orf37; Chromosome 6 open reading frame 37; D930050G01Rik; FA46A_HUMAN; FAM46A; Family with sequence similarity 46, member A; FLJ20037; FLJ31495; HBV X-transactivated gene 11 protein; HBV XAg-transactivated protein 11; Hypothetical protein LOC55603; OTTHUMP00000016782; Protein FAM46A; Retinal expressed gene C6orf37; RGD1311381; XTP11.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  神經生物學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Cow, )
產品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 50kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FAM46A
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:
Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The FAM46A gene product has been provisionally designated FAM46A pending further characterization.

Tissue Specificity:
Widely expressed, with preferential expression observed in the retina compared to other ocular tissues.

Similarity:
Belongs to the FAM46 family.

Database links:

Entrez Gene: 55603 Human

Entrez Gene: 212943 Mouse

Omim: 611357 Human

SwissProt: Q96IP4 Human

Unigene: 10784 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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