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Rabbit Anti-C19orf56/AF594 Conjugated antibody
Rabbit Anti-C19orf56/AF594 Conjugated antibody
C19orf56; Chromosome 19 open reading frame 56; ASTER_HUMAN; Hypothetical protein LOC51398; PTD008; UPF0139 membrane protein C19orf56.
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Product Name Anti-C19orf56/AF594
Chinese Name AF594标记的19号染色体开放阅读框56抗体
Alias C19orf56; Chromosome 19 open reading frame 56; ASTER_HUMAN; Hypothetical protein LOC51398; PTD008; UPF0139 membrane protein C19orf56.  
Research Area Tumour  Cell biology  Diabetes  
Immunogen Species Rabbit
Clonality Polyclonal
React Species
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 12kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C19orf56
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:
C19orf56 is a 106 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.

Subcellular Location:
Membrane.

Similarity:
Belongs to the UPF0139 (CGI-140) family.

Database links:

Entrez Gene: 51398 Human

SwissProt: Q9Y284 Human

SwissProt: Q6ZWX0 Mouse

Unigene: 108969 Human

Unigene: 657204 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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