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Product Name CCZ1 Chinese Name CCZ1蛋白抗体 Alias C7orf28A; CCZ1 vacuolar protein trafficking and biogenesis associated homolog (S. cerevisiae); CCZ1A; CGI-43; H_DJ1163J12.2; Vacuolar fusion protein CCZ1 homolog; CCZ1_HUMAN. Research Area Cell biology Developmental biology Immunogen Species Rabbit Clonality Polyclonal React Species (predicted: Human, Mouse, Rat, Pig, Horse, Rabbit, Sheep, ) Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 56kDa Cellular localization cytoplasmic The cell membrane Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human CCZ1: 51-150/482 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf28 gene product has been provisionally designated C7orf28 pending further characterization.
Subcellular Location:
Lysosome membrane.
Similarity:
Belongs to the CCZ1 family.
SWISS:
P86791
Gene ID:
51622
Database links:Entrez Gene: 51622 Human
Entrez Gene: 231874 Mouse
SwissProt: P86791 Human
SwissProt: Q8C1Y8 Mouse
Unigene: 530000 Human
Unigene: 320432 Mouse
Unigene: 137253 Rat
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