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Rabbit Anti-CCZ1 antibody
Rabbit Anti-CCZ1 antibody
C7orf28A; CCZ1 vacuolar protein trafficking and biogenesis associated homolog (S. cerevisiae); CCZ1A; CGI-43; H_DJ1163J12.2; Vacuolar fusion protein CCZ1 homolog; CCZ1_HUMAN.
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  • NO.:SL9543R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Pig,Horse,Rabbit,Sheep,)
    Applications:ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
  • Goods click count:15
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Details

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: 511088 Cow

Entrez Gene: 231874 Mouse

Entrez Gene: 360768 Rat

SwissProt: Q0VD30 Cow

SwissProt: P86791 Human

SwissProt: Q8C1Y8 Mouse

Unigene: 530000 Human

Unigene: 320432 Mouse

Unigene: 137253 Rat



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