Home > Product > Antibody > Rabbit Anti-C8orf70/FITC Conjugated antibody
C8orf70; Chromosome 8 open reading frame 70; F164A_HUMAN; fam164a; family with sequence similarity 164, member A; Hypothetical protein C8orf70; hypothetical protein LOC51101; Protein FAM164A; CGI 62; CGI-62.
Cat:
SL9666R-FITC
Species Reactivity:
Mouse,(predicted: Human,Rat,Dog,Pig,Cow,Horse,Rabbit,)
Immunogen:
KLH conjugated synthetic peptide derived from human CGI62/C8orf70
Format:
Lyophilized or Liquid
Storage instructions:
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 ant
Buffer:
0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
ICC=1:50-200IF=1:50-200not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Calculated MW:
36kDa
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Unit:
Price: $
Product PDFs
Datasheet:


background:
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf70 gene product has been provisionally designated C8orf70 pending further characterization.

Similarity:
Belongs to the ZC2HC1 family.
Contains 1 C2HSLCtype zinc finger.

Database links:

Entrez Gene: 51101 Human

Entrez Gene: 310244 Rat

SwissProt: Q96GY0 Human

Unigene: 271876 Human

Unigene: 8041 Rat



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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