Lectin PNA From Arachis hypogaea (peanut), Alexa Fluor™ 594 Conjugate
Citas y referencias (10)
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 ofMás información
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Número de catálogo
Cantidad
L32459
1 mg
Número de catálogo L32459
Precio (CLP)
229.091
Each
Añadir al carro de la compra
Cantidad:
1 mg
Precio (CLP)
229.091
Each
Añadir al carro de la compra
Lectin PNA is specific for terminal β-galactose. It will agglutinate human erythrocytes, but only after neuraminidase treatment.
For Research Use Only. Not for use in diagnostic procedures.
Especificaciones
Tipo de etiquetaAlexa Fluor Dyes
Línea de productosAlexa Fluor
Subtipo de proteínaLectins
Cantidad1 mg
Condiciones de envíoRoom Temperature
FuentePeanut
ConjugadoAlexa Fluor 594
FormularioLyophilized
Unit SizeEach
Contenido y almacenamiento
Store in freezer (-5 to -30°C) and protect from light.
Citations & References (10)
Citations & References
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.