GFP-Tag Polyclonal Antibody

Elabscience
Product Code: E-AB-20050
Product Group: Primary Antibodies
Supplier: Elabscience
CodeSizePrice
E-AB-20050-30uL30uL£125.00
Quantity:
E-AB-20050-60uL60uL£146.00
Quantity:
E-AB-20050-120uL120uL£196.00
Quantity:
E-AB-20050-200uL200uL£216.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Application: Western Blot (WB)
Shipping:
Ice packs
Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Images

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Western Blot analysis of 1ug GFP fusion protein using GFP-Tag Polyclonal Antibody at dilution of 1) 1:5000 2) 1:1000.

Western Blot analysis of 1ug GFP fusion protein using GFP-Tag Polyclonal Antibody at dilution of 1) 1:5000 2) 1:1000.

Documents

Further Information

Abbreviation:
GFP-Tag
Background:
Protein tags are protein or peptide sequences located either on the C- or N- terminal of the target protein, which facilitates one or several of the following characteristics: solubility, detection, purification, localization and expression. Green fluorescence protein(GFP) is a protein composed of 238 amino acid residues(26.9kDa) derived from the Jellyfish Aequorea victoria, which emits green light(emission peak at 509nm) when excited by blue light(excitation peak at 395nm). GFP has become an invaluable tool in cell biology research, since its intrinsic fluorescence can be visualized in living cells. EGFP contains the double-amino-acid substitutions Phe-64 to Leu and Ser-65 to Thr(previously published as GFPmut1). In contrast to wtGFP, EGFP has a single, strong, red-shifted excitation peak at 488nm. GFPmut1 fluoresces 35-fold more intensely than wtGFP when excited at 488nm, due to an increase in its extinction coefficient(Em).
Buffer:
PBS with 0.02% sodium azide and 50% glycerol pH 7.4.
Concentration:
1 mg/mL
Conjugation:
Unconjugated
Dilution:
WB 1:5000-1:10000
Immunogen:
Recombinant Protein
Purification method:
Affinity purification
Target Synonym:
GFP;Green fluorescent protein

References

  • https://link.springer.com/article/10.1007/s12035-018-1464-3