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Rabbit Anti-FAM194B/AP Conjugated antibody
Rabbit Anti-FAM194B/AP Conjugated antibody
C3orf44; F194B_HUMAN; Family with sequence similarity 194, member A; MGC39662; Protein FAM194A.
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  • NO.:SL14774R-AP
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,
    Applications:WB IHC-P IHC-F ICC
    concentration:1mg/ml
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Product Name Anti-FAM194B/AP
Chinese Name 碱性磷酸酶(AP)标记的FAM194B蛋白抗体
Alias C3orf44; F194B_HUMAN; Family with sequence similarity 194, member A; MGC39662; Protein FAM194A.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, 
Applications 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.
Molecular weight 82kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FAM194B
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:
FAM194B is a 696 amino acid protein that belongs to the FAM194 family and is alternatively spliced created two isoforms. The gene encoding FAM194B maps to human chromosome 13, which comprises nearly 4% of human DNA and contains about 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival.

Function:
The function of this protein remains unknown.

Similarity:
Belongs to the FAM194 family.

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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