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Merck
CN

411423

Mouse Anti-Human IgA, Secretory (HP6141)

liquid, clone HP6141, Calbiochem®

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关于此项目

NACRES:
NA.74
UNSPSC Code:
12352203
Clone:
HP6141, monoclonal
Species reactivity:
-
Application:
Citations:
2
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biological source

mouse

antibody form

purified immunoglobulin

antibody product type

secondary antibodies

clone

HP6141, monoclonal

form

liquid

does not contain

preservative

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, avoid repeated freeze/thaw cycles

isotype

IgG1

shipped in

wet ice

storage temp.

−20°C

Quality Level

General description

Purified mouse monoclonal IgG. Recognizes human IgA secretory subunit.
This Mouse Anti-Human IgA, Secretory (HP6141) is validated for use in ELISA for the detection of Human IgA, Secretory.

Packaging

Please refer to vial label for lot-specific concentration.

Other Notes

Can be used as a capture antibody for ELISA at 10 µg/ml in PBS without carrier protein. Antibody should be titrated for optimal results in individual systems.



Cross-reactivity by ELISA against human myeloma proteins:

Human IgG: <0.01%

Human IgE: <0.01%

Human IgM: <0.01%

Human IgA1: <0.01%

Human IgA2: <0.01%

Human secretory IgA: 100%
Hamilton, R.G., 1990. Ann. Biol. Clin.48, 473.
Fasullo, F.J., et al. 1989. Clin. Chem.35, 364.
Reimer, C.B., et al. 1989. Immunol. Letters21, 209.

Legal Information

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

Disclaimer

Toxicity: Standard Handling (A)

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存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Alba Escalera et al.
iScience, 27(3), 109210-109210 (2024-03-04)
Despite multiple research efforts to characterize coronavirus disease 2019 (COVID-19) in humans, there is no clear data on the specific role of mucosal immunity on COVID-19 disease. Here, we longitudinally profile the antibody response against severe acute respiratory syndrome coronavirus
Hailey Hornsby et al.
Nature communications, 14(1), 5065-5065 (2023-08-22)
Pronounced immune escape by the SARS-CoV-2 Omicron variant has resulted in many individuals possessing hybrid immunity, generated through a combination of vaccination and infection. Concerns have been raised that omicron breakthrough infections in triple-vaccinated individuals result in poor induction of

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