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Rabbit Anti-C19orf55/Cy5.5 Conjugated antibody
Rabbit Anti-C19orf55/Cy5.5 Conjugated antibody
Chromosome 19 open reading frame 55; Uncharacterized protein C19orf55; Uncharacterized protein C19orf55 homolog; CS055_HUMAN.
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  • NO.:SL13789R-Cy5.5
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,Mouse,(predicted: Rat,Pig,Cow,)
    Applications:ICC IF
    concentration:1mg/ml
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Product Name Anti-C19orf55/Cy5.5
Chinese Name Cy5.5标记的19号染色体开放阅读框55抗体
Alias Chromosome 19 open reading frame 55; Uncharacterized protein C19orf55; Uncharacterized protein C19orf55 homolog; CS055_HUMAN.  
Research Area Tumour  Cell biology  Neurobiology  Diabetes  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, Mouse,  (predicted: Rat, Pig, Cow, )
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 51kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C19orf55
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:
C19orf55 is a 480 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

Function:
The function of this protein remains unknown.

Database links:

Entrez Gene: 148137 Human

SwissProt: Q2NL68 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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