Products for Research Use Only

TCF4 Antibody (RPE)

CAT: 0013-GTR18028136Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18028136Size:100 µg
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Description
Rabbit polyclonal antibody against TCF4 conjugated to RPE
Product Name Alternative
TCF-4, MGC149723, PTHS, Class B basic helix-loop-helix protein 19, bHLHb19, SEF 2, SL3 3 enhancer factor 2, SEF2 1, ITF-2, E2 2, SEF2 1A, BHLHB19, MGC149724, ITF 2, Transcription factor 4, TCF 4, SEF-2, SEF2 1B, Immunoglobulin transcription factor 2, SL3-3 enhancer factor 2, SEF2, ITF2, ITF2_HUMAN
UniProt
P15884
Reactivity
Human, Mouse
Immunogen
Synthetic peptide from the C-terminal of Human TCF4 (500-600 aa), conjugated to Keyhole Limpet Haemocyanin (KLH) .
Target
TCF4
Clonality
Polyclonal
Conjugation
RPE
Field of Research
Metabolism Research
Purification
Peptide Affinity Purified
Concentration
1 mg/ml
Dilution
WB (1:1000) ; IHC (1:50)
Molecular Weight
71 kDa, 45 kDa
Storage Conditions
Conjugated antibodies should be stored according to the product label
Notes
For research use only.
Applications Notes
A 1:1000 dilution was sufficient for detection of TCF4 in 15 μg of mouse liver cell lysates by ECL immunoblot analysis using goat anti-rabbit IgG:HRP as the secondary antibody.
Tested Applications
IHC, WB
NCBI Accession Number
NP_001077431.1
Host or Source
Rabbit
Preservative
95.46mM Phosphate, 2.48mM MES and 2mM EDTA
Entrez
6925

UniProtKB · P15884

Transcription factor 4

ITF2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P15884
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
TCF4
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
TCF-4
EC number
—
Processing
—
Secondary accessions
B3KT62, B3KUC0, B4DT37, B4DUG3, B7Z5M6, B7Z6Y1, G0LNT9, G0LNU0, G0LNU1, G0LNU2, G0LNU4, G0LNU5, G0LNU8, G0LNU9, G0LNV0, G0LNV1, G0LNV2, H3BPQ1, Q08AP2, Q08AP3, Q15439, Q15440, Q15441
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Molecular function

ActivatorDNA-binding

Coding sequence diversity

Alternative splicing

Disease

Corneal dystrophyDisease variantEpilepsyIntellectual disabilityPrimary microcephaly

Biological process

DifferentiationNeurogenesisTranscriptionTranscription regulation

Cellular component

Nucleus

PTM

Phosphoprotein