C6orf191抗体;bA174C7.4; C6orf191; TM244_HUMAN; Chromosome 6 open reading frame 191; Putative transmembrane protein C6orf191

Rabbit

C6orf191

Mouse

Human;Pig;Cow;Horse;Sheep;

WB=1:500-2000

Predicted molecular weight: 15kDa
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

KLH conjugated synthetic peptide derived from human C6orf191:31-128/128 

1mg/ml

affinity purified by Protein A

Polyclonal Antibody

IgG

Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

细胞生物  免疫学  

WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 ICC=1:100-500 IF=1:100-500 

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson’s disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf191 gene product has been provisionally designated C6orf191 pending further characterization.

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