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Rabbit Anti-FAM194A/PE-Cy3 Conjugated antibody
Rabbit Anti-FAM194A/PE-Cy3 Conjugated antibody
C3orf44; F194A_HUMAN; Family with sequence similarity 194, member A; MGC39662; Protein FAM194A.
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  • NO.:SL14773R-PE-Cy3
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Mouse,(predicted: Human,Rat,Pig,)
    Applications:ICC IF
    concentration:1mg/ml
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Product Name Anti-FAM194A/PE-Cy3
Chinese Name PE-Cy3标记的FAM194A蛋白抗体
Alias C3orf44; F194A_HUMAN; Family with sequence similarity 194, member A; MGC39662; Protein FAM194A.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Mouse,  (predicted: Human, Rat, Pig, )
Applications ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 75kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FAM194A
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage 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.
Product Detail background:
FAM194A is a 663 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding FAM194A maps to human chromosome 3, which is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Function:
The function of this protein remains unknown.

Similarity:
The function of this protein remains unknown.

Database links:

Entrez Gene: 131831 Human

SwissProt: Q7L0X2 Human

Unigene: 147128 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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