Lectin PNA From <i>Arachis hypogaea </i>(peanut), Alexa Fluor&trade; 594 Conjugate
Invitrogen™

Lectin PNA From Arachis hypogaea (peanut), Alexa Fluor™ 594 Conjugate

Lectin PNA is specific for terminal β-galactose. It will agglutinate human erythrocytes, but only after neuraminidase treatment.View complete list ofAfficher plus
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RéférenceQuantité
L324591 mg
Référence L32459
Prix (EUR)
260,00
Each
Quantité:
1 mg
Prix (EUR)
260,00
Each
Lectin PNA is specific for terminal β-galactose. It will agglutinate human erythrocytes, but only after neuraminidase treatment.

View complete list of fluorescent dye-conjugated lectins ›

For Research Use Only. Not for use in diagnostic procedures.
Spécifications
Type d’étiquetteAlexa Fluor Dyes
Gamme de produitsAlexa Fluor
Sous-type de protéineLectins
Quantité1 mg
Conditions d’expéditionRoom Temperature
SourcePeanut
ConjuguéAlexa Fluor 594
FormeLyophilized
Unit SizeEach
Contenu et stockage
Store in freezer (-5 to -30°C) and protect from light.

Citations et références (10)

Citations et références
Abstract
Localization of sphingosine kinase-1 in mouse sperm acrosomes.
Authors:Matsumoto K, Banno Y, Murate T, Akao Y, Nozawa Y
Journal:J Histochem Cytochem
PubMed ID:15684337
Sphingosine kinase (SPHK) catalyzes sphingosine phosphorylation to form a bioactive lipid mediator, sphingosine-1-phosphate (S1P). In the current study, we report the presence of SPHK-1 in mouse spermatozoa. SPHK-1 was localized to the acrosomes of spermatozoa, and its expression was proven by RT-PCR and Western blot analysis. SPHK activity of mouse ... More
Substantial restoration of night vision in adult mice with congenital stationary night blindness.
Authors:
Journal:Mol Ther Methods Clin Dev
PubMed ID:34401402
Shared developmental programme strongly constrains beak shape diversity in songbirds.
Authors:
Journal:Nat Commun
PubMed ID:24739280
Therapeutic Regeneration of Lymphatic and Immune Cell Functions upon Lympho-organoid Transplantation.
Authors:
Journal:Stem Cell Reports
PubMed ID:31155505
Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy.
Authors:
Journal:PLoS One
PubMed ID:24671090