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Antibody used in WB on Human Placenta at 0.2-1 ug/ml.
Antibody used in WB on Human Placenta at 0.2-1 ug/ml.

ZNF141 Antibody

CATALOG NUMBER: 25-427

Clonality:
Polyclonal
Tested Applications:
ELISA, WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ZNF141.
Conjugate:
Unconjugated
Tested Applications:
ELISA, WB
Application Note:
ZNF141 antibody can be used for detection of ZNF141 by ELISA at 1:312500. ZNF141 antibody can be used for detection of ZNF141 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. 1309 - Human Placenta Lysate
Predicted Molecular Weight:
55 kDa
Purification:
Antibody is purified by peptide affinity chromatography method.
Clonality:
Polyclonal
physical-state:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store ZNF141 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
ZNF141
Additional Names:
ZNF141, D4S90, pHZ-44, PAPA6
Protein Accession Number:
NP_003432
Protein Gi Number:
4507993
Ncbi Gene Id Number:
7700
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
Zinc finger encoding genes would be good candidates for being involved in the multiple developmental defects associated with chromosomal aneusomy--because of their role as transcriptional regulators, their abundance in the genome and their known association with specific developmental disorders. A zinc finger encoding cDNA (ZNF141) of the C2-H2/KRAB subfamily has been mapped to the 4p- (Wolf-Hirschhorn) syndrome (WHS) chromosome region. ZNF141 was expressed ubiquitously at low levels in the analysed tissue. The identification of a candidate gene for a chromosomal aneusomy syndrome belonging to a class of evolutionary conserved genes will provide options for studying its normal and abnormal expression during mammalian embryogenesis.
Background Reference 1:
Varrault, A., (1998) Proc. Natl. Acad. Sci. U.S.A. 95 (15), 8835-8840.

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

25-427

List Size:
100 ul

List Price:

$519.00

Datasheet
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