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MABE1824

Sigma-Aldrich

Anti-LbCpf1 Antibody, clone 2D5-6G11

clone 2D5-6G11, from mouse

Sinonimo/i:

Cpf1

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About This Item

Codice UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.43

Origine biologica

mouse

Forma dell’anticorpo

purified immunoglobulin

Tipo di anticorpo

primary antibodies

Clone

2D5-6G11, monoclonal

Reattività contro le specie

Lachnospiraceae, bacteria

Confezionamento

antibody small pack of 25 μg

tecniche

western blot: suitable

Isotipo

IgG1κ

modifica post-traduzionali bersaglio

unmodified

Descrizione generale

CRISPR-associated endonuclease Cas12a (UniProt: A0A182DWE3; also known as CRISPR-associated endonuclease Cpf1; Lbcpf1) is a single crRNA-guided endonuclease of the class 2 CRISPR-Cas system that lacks tracrRNA and undergoes large conformational changes upon crRNA binding. Cpf1 has several features that can distinguish it from Cas9. Unlike Cas9 that uses dual-guide RNAs, Cpf1 is guided by a crRNA. It recognizes a T-rich PAM (T-rich protospacer adjacent motif), whereas Cas9 favors a G-rich PAM and Cpf1 generates staggered ends at its PAM-distal region, but Cas9 creates blunt ends at its PAM-proximal region. Cpf1 displays higher targeting specificity in mammalian cells when compared to Cas9. It has been shown that depending on the PAM sequences, LbCpf1 can undergo conformational changes to form altered interactions with the PAM-containing DNA duplexes, hence achieving the relaxed PAM recognition. (Ref.: Zetsche, B., et al. (2015). Cell 163(3); 759-77; Yamano, T., et al. (2017). Mol. Cell 67(4); 633-645; Gao, P., et al. (2016). Cell Res. 26(8); 901-913).

Specificità

Clone 2D5-6G11 specifically detects CRISPR-associated endonuclease Cas12a (LbCpf1).

Immunogeno

Epitope: N-terminus
His-tagged recombinant fragment from the N-terminal region of Lachnospiracea bacteria.

Applicazioni

Anti-LbCpf1, clone 2D5-6G11 Antibody, Cat. No. MABE1824, is a highly specific mouse monoclonal antibody that targets LbCpf1 and has been tested for use in Western Blotting.
Research Category
Epigenetics & Nuclear Function
Western Blotting Analysis: Various dilutions from a representative lot detected LbCpf1 in lysates from HEK293 cells expressing HA-tagged LbCpf1 (Courtesy of Stefan Schuchner, Ph.D. and Egon Ogris, M.D., Medical University of Vienna, Austria).

Qualità

Evaluated by Western Blotting in HEK293 cells expressing HA-tagged LbCpf1.

Western Blotting Analysis: 1 µg/mL of this antibody detected LbCpf1 in lysate from HEK293 cells expressing HA-tagged LbCpf1.

Descrizione del bersaglio

~144 kDa observed; 143.03 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

Stato fisico

Format: Purified
Protein G purified
Purified mouse monoclonal antibody IgG1 in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Stoccaggio e stabilità

Stable for 1 year at 2-8°C from date of receipt.

Altre note

Concentration: Please refer to lot specific datasheet.

Esclusione di responsabilità

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Audrey M V Ah-Fong et al.
Molecular plant pathology, 22(6), 737-752 (2021-03-17)
Phytophthora infestans is a destructive pathogen of potato and a model for investigations of oomycete biology. The successful application of a CRISPR gene editing system to P. infestans is so far unreported. We discovered that it is difficult to express CRISPR/Cas9

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