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Merck

AB986

Anti-β Galactosidase Antibody, bacterial

serum, Chemicon®

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Informacje o tej pozycji

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
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Nazwa produktu

Anti-β Galactosidase Antibody, bacterial, serum, Chemicon®

biological source

rabbit

conjugate

unconjugated

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

E. coli, vertebrates

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

Gene Information

human ... GLB1(2720)

Application

Anti-β Galactosidase Antibody, bacterial detects level of β Galactosidase & has been published & validated for use in ELISA, IP, WB, IH.
Immunoblotting: 1:500-1:2,000

Immunoprecipitation

Immunohistochemistry (Zhang, 2002)

ELISA: 1:2,000-1:10,000 when tested against 1 μg of immunogen by a standard sandwich ELISA.

Optimal working dilutions must be determined by the end user.
Research Category
Metabolism
Research Sub Category
Enzymes & Biochemistry

Biochem/physiol Actions

Specific for Beta galactosidase from E coli by IEP. May cross react with Beta galactosidase from other species.

Disclaimer

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.

General description

The previously assigned protein identifier P16279 has been merged into P16278. Full details can be found on the UniProt database.

Immunogen

Beta galactosidase from E-coli.
Epitope: bacterial

Physical form

Rabbit antisera prepared by delipidation and defibrination. Lyophilized. Reconstitute with 2 mL of sterile deionized water. Contains 0.02M Potassium Phosphate, 0.15M NaCl and 0.01% sodium azide after reconstitution.

Preparation Note

Maintain lyophilized material at 2-8°C for up to 12 months. After reconstitution maintain in undiluted aliquots at -20°C for up to 6 months. Avoid repeated freeze/thaw cycles.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3

Klasa składowania

11 - Combustible Solids

wgk

WGK 3


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Odwiedź Bibliotekę dokumentów

Dushani L Palliyaguru et al.
Free radical biology & medicine, 101, 116-128 (2016-11-05)
Small molecules of plant origin offer presumptively safe opportunities to prevent carcinogenesis, mutagenesis and other forms of toxicity in humans. However, the mechanisms of action of such plant-based agents remain largely unknown. In recent years the stress responsive transcription factor
J Sedý et al.
Developmental dynamics : an official publication of the American Association of Anatomists, 235(4), 1081-1089 (2006-02-24)
ER81, a member of the ETS family of transcription factors, is involved in processes of specification of neuronal identity, control of sensory-motor connectivity, and differentiation of muscle spindles. Spindles either degenerate or are abnormal in mutant mice lacking ER81. We
Thomas Visone et al.
Biology of reproduction, 81(3), 571-579 (2009-05-22)
In murine testes, only Sertoli cells express the cathepsin L (Ctsl) gene, and this expression is restricted to stages V-VIII of the cycle. Our previous transgenic analysis of Tg (-2065/+977) demonstrated that this expression is regulated by a approximately 2-kb
Susanne Walter et al.
Acta neuropathologica, 137(2), 239-257 (2018-11-15)
Brain accumulation and aggregation of amyloid-β (Aβ) peptides is a critical step in the pathogenesis of Alzheimer's disease (AD). Full-length Aβ peptides (mainly Aβ1-40 and Aβ1-42) are produced through sequential proteolytic cleavage of the amyloid precursor protein (APP) by β-
Mesodiencephalic dopaminergic neuronal differentiation does not involve GLI2A-mediated SHH-signaling and is under the direct influence of canonical WNT signaling.
Mesman, S; von Oerthel, L; Smidt, MP
Testing null

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