ZNF141 anticorps

N° du produit ABIN2458313

L’anticorps anti-ZNF141 Polyclonal Lapin est utilisé pour la détection de ZNF141 dans des échantillons de Humain. Il a été validé pour WB et ELISA.

Aperçu rapide pour ZNF141 anticorps (ABIN2458313)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ZNF141 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-ZNF141 anticorps

Purification: Antibody is purified by peptide affinity chromatography method.

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

Information d'application

Indications d'application: 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

Stockage

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.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

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

Détails sur ZNF141

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

Autre désignation: ZNF141

Sujet: 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.

Poids moléculaire: 55 kDa

ID gène: 7700

NCBI Accession: NP_003432

UniProt: Q15928