ZNF141 antibody

Catalog No. ABIN2458313

The Rabbit Polyclonal anti-ZNF141 antibody is suitable to detect ZNF141 in samples from Human. It has been validated for WB and ELISA.

Quick Overview for ZNF141 antibody (ABIN2458313)

Target: ZNF141 (Zinc Finger Protein 141 (ZNF141))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ZNF141 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-ZNF141 Antibody

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ZNF141.

Application Details

Application Notes: 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.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store ZNF141 antibody at -20 °C.

Target Details for ZNF141

Target: ZNF141 (Zinc Finger Protein 141 (ZNF141))

Alternative Name: ZNF141

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.

Molecular Weight: 55 kDa

Gene ID: 7700

NCBI Accession: NP_003432

UniProt: Q15928