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TCF4 Rabbit Polyclonal Antibody (Biotin)

CAT: 0013-GTR18338830Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18338830Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
TCF4 Rabbit Polyclonal Antibody (Biotin)
Product Name Alternative
E2-2, ITF2, PTHS, SEF2, CDG2T, FECD3, ITF-2, SEF-2, TCF-4, SEF2-1, SEF2-1A, SEF2-1B, SEF2-1D, bHLHb19
UniProt
P15884
Immunogen
The immunogen is a synthetic peptide directed towards the N terminal region of human TCF4
Clonality
Polyclonal
Conjugation
Biotin
Sequence
Synthetic peptide located within the following region: MHHQQRMAALGTDKELSDLLDFSAMFSPPVSSGKNGPTSLASGHFTGSNV
Form
Liquid. Purified antibody supplied in 1x PBS buffer.
Molecular Weight
71kDa
Storage Conditions
All conjugated antibodies should be stored in light-protected vials or covered with a light protecting material (i.e. aluminum foil) . Conjugated antibodies are stable for at least 12 months at 4C. If longer storage is desired (24 months), conjugates may be diluted with up to 50% glycerol and stored at -2°C to -8°C. Freezing and thawing conjugated antibodies will compromise enzyme activity as well as antibody binding.
Notes
For research use only.
Prediction Reactivity
Equine, Guinea pig, Human, Mouse
Tested Applications
WB
NCBI Accession Number
NP_003190
Host or Source
Rabbit
Preservative
Liquid. Purified antibody supplied in 1x PBS buffer.

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

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