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Rabbit Anti-CCDC126/AF488 Conjugated antibody
Rabbit Anti-CCDC126/AF488 Conjugated antibody
LOC90693;alpha 1,3(6) mannosylglycoprotein; beta 1,6 N acetyl glucosaminyltransferase like; CC126_HUMAN; Ccdc126; coiled coil domain containing 126; Coiled-coil domain-containing protein 126; FLJ23031; MGC104248; OTTHUMP00000158577.
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Details

Product Name Anti-CCDC126/AF488
Chinese Name AF488标记的卷曲螺旋结构域蛋白126抗体
Alias LOC90693; alpha 1,3(6) mannosylglycoprotein; beta 1,6 N acetyl glucosaminyltransferase like; CC126_HUMAN; Ccdc126; coiled coil domain containing 126; Coiled-coil domain-containing protein 126; FLJ23031; MGC104248; OTTHUMP00000158577.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
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 13kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human CCDC126
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:
CCDC126 is a 140 amino acid secreted protein encoded by a gene mapping to human chromosome 7. 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.

Subcellular Location:
Secreted.

Database links:

Entrez Gene: 90693 Human

SwissProt: Q96EE4 Human

Unigene: 232296 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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