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Merck
CN

AP1181

Anti-TLR7 Mouse mAb (2C9)

liquid, clone 2C9, Calbiochem®

别名:

Anti-Toll-like Receptor 7

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关于此项目

NACRES:
NA.41
UNSPSC Code:
12352203
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产品名称

Anti-TLR7 Mouse mAb (2C9), liquid, clone 2C9, Calbiochem®

biological source

mouse

antibody form

purified antibody

antibody product type

primary antibodies

clone

2C9, monoclonal

form

liquid

does not contain

preservative

species reactivity

human

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
avoid repeated freeze/thaw cycles

dilution

(ELISA
Immunoblotting (1-5 µg/mL))

isotype

IgG2b

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... TLR7(51284)

Analysis Note

Positive Control
IMR32 cells

Application


ELISA (see comments)
Immunoblotting (1-5 g/ml)

Disclaimer

Toxicity: Regulatory Review (Z)

General description

Purified mouse monoclonal antibody. Recognizes the ~120 kDa TLR7 protein.
Recognizes the ~120 kDa TLR7 protein in IMR32 cells.
This Anti-TLR7 Mouse mAb (2C9) is validated for use in ELISA, Immunoblotting for the detection of TLR7.

Immunogen

A recombinant polypeptide corresponding to amino acids of 27-127 human TLR7, expressed as a GST fusion protein

Other Notes

For ELISA, this antibody can be used as the capture antibody; recommended concentration is 10 ng/ml, 1 µg/well, 100 µl total volume. Variables associated with assay conditions will dictate the proper working dilution.

Physical form

In PBS, pH 7.2.

Preparation Note

Following initial thaw, aliquot and freeze (-20°C).

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

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存储类别

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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Yang Gu et al.
Medical science monitor : international medical journal of experimental and clinical research, 26, e923104-e923104 (2020-05-27)
BACKGROUND The metabolic processing of ellagic acid (EA) by cytochrome P450s (CYP450s) expressed in the intestines is unclear. This study aimed to investigate the effects of CYP450s that are highly expressed in HIEC cells on metabolic activity of EA. MATERIAL

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