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[KD Validated] Anti-TEAD1 Rabbit mAb [19Q78B07]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R021547
20µL ¥738.00
50µL ¥1380.00
100µL ¥2280.00

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[KD Validated] Anti-TEAD1 Rabbit mAb [19Q78B07]
[KD Validated] Anti-TEAD1 Rabbit mAb [19Q78B07]
[KD Validated] Anti-TEAD1 Rabbit mAb [19Q78B07]
[KD Validated] Anti-TEAD1 Rabbit mAb [19Q78B07]
Product Name[KD Validated] Anti-TEAD1 Rabbit mAb
DescriptionPurified Recombinant Rabbit Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, FC, IF (Cell)/ICC
DilutionWB 1:1,000~1:5,000; FC 1:200~1:2,000; IF 1:100~1:1,000
ReactivityHuman, Mouse, Rat
HostRabbit
ClonalityMonoclonal
Clone No.19Q78B07
IsotypeIgG
LabelUnconjugated
ImmunogenA synthesized peptide derived from human TEAD1
FormatAffinity purified monoclonal antibody supplied in PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
SynonymsTEAD1; TEA Domain Transcription Factor 1; TEF-1; TCF13; TEA Domain Family Member 1 (SV40 Transcriptional Enhancer Factor); Transcriptional Enhancer Factor TEF-1; Transcriptional Enhancer Factor 1; Transcription Factor 13; Protein GT-IIC; NTEF-1; TCF-13; TEAD-1; AA; Atrophia Areata, Peripapillary Chorioretinal Degeneration; TEA Domain Family Member 1; REF1; TEF1.
Molecular weightCalculated MW: 48 kDa, Observed MW: 52 kDa
Uniprot ID P28347
Gene ID 7003
StorageShipped on wet ice. Store at -20℃. Stable for 12 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
Precautions[KD Validated] Anti-TEAD1 Rabbit mAb [19Q78B07] is for research use only and not for use in diagnostic or therapeutic procedures.
Background 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. [provided by RefSeq, May 2010]
Cellular Location Nucleus.
Tissue Location Preferentially expressed in skeletal muscle. Lower levels in pancreas, placenta, and heart.

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