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Rabbit Anti-FAM114A2/PE-Cy7 Conjugated antibody
Rabbit Anti-FAM114A2/PE-Cy7 Conjugated antibody
133K02; C5orf3; Chromosome 5 open reading frame 3; F1142_HUMAN; FAM114A2; Family with sequence similarity 114 member A2; Hypothetical protein LOC10827; Protein FAM114A2.
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Product Name Anti-FAM114A2/PE-Cy7
Chinese Name PE-Cy7标记的FAM114A2蛋白抗体
Alias 133K02; C5orf3; Chromosome 5 open reading frame 3; F1142_HUMAN; FAM114A2; Family with sequence similarity 114 member A2; Hypothetical protein LOC10827; Protein FAM114A2.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, )
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 55kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FAM114A2
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:
FAM114A2 is a 505 amino acid protein that belongs to the FAM114 family. FAM114A2 is post-translationally phosphorylated at serine 146 and threonine 207. The gene encoding FAM114A2 maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Similarity:
Belongs to the FAM114 family.

Database links:

Entrez Gene: 10827 Human

SwissProt: Q9NRY5 Human

Unigene: 166551 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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