TEAD1 Antilichaam

This gene encodes a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor. Mutations in this gene cause Sveinsson's chorioretinal atrophy. Additional transcript variants have been described but their full-length natures have not been experimentally verified.

7003

P28347

Human, Mouse

Recombinant fusion protein containing a sequence corresponding to amino acids 135-215 of human TEAD1 (NP_068780.2) .

Unconjugated

Primary Antibodies

Cell Cycle, Transcription

Affinity purification

HeLa

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 48kDa

IgG

TEAD1

MCF-7

Mouse kidney

Mouse heart3

TEA domain family member 1 (SV40 transcriptional enhancer factor)

Homo sapiens

TEAD1, AA, REF1, TCF13, TEF-1, NTEF-1, TCF-13, TEAD-1

WB, IHC, IF, ChIP

Liquid