Lectin PNA From Arachis hypogaea (peanut), Alexa Fluor™ 594 Conjugate
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 of자세히 알아보기
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카탈로그 번호수량
L324591 mg
카탈로그 번호 L32459
제품 가격(KRW)
269,000
キャンペーン価格
Ends: 31-Dec-2025
316,000
할인액 47,000 (15%)
Each
카트에 추가하기
수량:
1 mg
제품 가격(KRW)
269,000
キャンペーン価格
Ends: 31-Dec-2025
316,000
할인액 47,000 (15%)
Each
카트에 추가하기
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.
사양
라벨 유형Alexa Fluor Dyes
제품라인Alexa Fluor
단백질 아형Lectins
수량1 mg
배송 조건Room Temperature
소스Peanut
콘주게이트Alexa Fluor 594
형태Lyophilized
Unit SizeEach
구성 및 보관
Store in freezer (-5 to -30°C) and protect from light.

인용 및 참조 문헌 (10)

인용 및 참조 문헌
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