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Rabbit Anti-C3orf33/AF647 Conjugated antibody
Rabbit Anti-C3orf33/AF647 Conjugated antibody
AP-1 activity suppressor; E130311K13Rik; FLJ31139; MSTP052; RIKEN cDNA E130311K13; Uncharacterized protein C3orf33; CC033_HUMAN.
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  • NO.:SL9828R-AF647
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,(predicted: Mouse,Rat,Pig,Rabbit,Sheep,)
    Applications:IF
    concentration:1mg/ml
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Product Name Anti-C3orf33/AF647
Chinese Name AF647标记的3号染色体开放阅读框33抗体
Alias AP-1 activity suppressor; E130311K13Rik; FLJ31139; MSTP052; RIKEN cDNA E130311K13; Uncharacterized protein C3orf33; CC033_HUMAN.  
Research Area Tumour  Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human,  (predicted: Mouse, Rat, Pig, Rabbit, Sheep, )
Applications IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 34kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C3orf33
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:
C3orf33, also known as FLJ31139, is a 294 amino acid single-pass membrane protein encoded by a gene that maps to human chromosome 3q25.31. Chromosome 3 is made up of approximately 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.

Subcellular Location:
Membrane; Single-pass membrane protein

Database links:

Entrez Gene: 285315 Human

SwissProt: Q6P1S2 Human

Unigene: 350846 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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