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HPA029695

Sigma-Aldrich

Anti-GPR132 antibody produced in rabbit

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution, ab2

Synonym(s):

Anti-G protein-coupled receptor 132, Anti-G2A, Anti-SIIR, Anti-p21, Anti-pp21

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1 KIT
CN¥11,569.45
5 X 1 KIT
CN¥46,289.42

CN¥11,569.45

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1 KIT
CN¥11,569.45
5 X 1 KIT
CN¥46,289.42

About This Item

UNSPSC Code:
12352203
Human Protein Atlas Number:
HPA029695
NACRES:
NA.41

CN¥11,569.45

Please contact Customer Service for Availability
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biological source

rabbit

Quality Level

100

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

product line

Prestige Antibodies® Powered by Atlas Antibodies

form

buffered aqueous glycerol solution

species reactivity

human

technique(s)

immunohistochemistry: 1:20- 1:50

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feature

CE compliant, powder-free: no, standard type EN 374 (cat. III), latex free, standard type EN 388 (cat. III), reusable

feature

CE compliant, latex free, powder-free: no, reusable, standard type EN 374 (cat. III), standard type EN 388 (cat. III)

feature

CE compliant, latex free, powder-free: no, reusable, standard type EN 374 (cat. III), standard type EN 388 (cat. III)

feature

CE compliant, latex free, powder-free: no, reusable, standard type EN 374 (cat. III), standard type EN 388 (cat. III)

material

black (fluorocarbon rubber), black gloves

material

black (fluorocarbon rubber), black gloves

material

black (fluorocarbon rubber), black gloves

material

black butyl rubber , black gloves

manufacturer/tradename

KCL 890

manufacturer/tradename

KCL 890

manufacturer/tradename

KCL 890

manufacturer/tradename

KCL 897

packaging

pack of 1 pair

packaging

pack of 1 pair

packaging

pack of 1 pair

packaging

pack of 1 pair

size

XL (11)

size

S (8)

size

L (10)

size

M

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

sterility

non-sterile

Immunogen

G protein-coupled receptor 132 recombinant protein epitope signature tag (PrEST)

Application

All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry.

The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. We also provide Prestige Antibodies® protocols and other useful information.

Features and Benefits

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

Physical form

Solution in phosphate-buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide.

Other Notes

Corresponding Antigen APREST78146

Legal Information

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

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.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

常规特殊物品

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    Certificates of Analysis (COA)

    Lot/Batch Number
    R28539

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    Min-Sik Kim et al.
    Journal of the American Society for Mass Spectrometry, 21(9), 1606-1611 (2010-05-21)
    Shotgun proteomics has been used extensively for characterization of a number of proteomes. High-resolution Fourier transform mass spectrometry (FTMS) has emerged as a powerful tool owing to its high mass accuracy and resolving power. One of its major limitations, however
    Mark V Ivanov et al.
    Journal of proteome research, 13(4), 1911-1920 (2014-02-28)
    Data-dependent tandem mass spectrometry (MS/MS) is one of the main techniques for protein identification in shotgun proteomics. In a typical LC-MS/MS workflow, peptide product ion mass spectra (MS/MS spectra) are compared with those derived theoretically from a protein sequence database.
    Henrik Molina et al.
    Analytical chemistry, 80(13), 4825-4835 (2008-06-11)
    Electron transfer dissociation (ETD) is a recently introduced mass spectrometric technique which has proven to be an excellent tool for the elucidation of labile post-translational modifications such as phosphorylation and O-GlcNAcylation of serine and threonine residues. However, unlike collision induced
    Leslie Muller et al.
    Proteomics, 16(23), 2953-2961 (2016-10-18)
    Sample preparation, typically by in-solution or in-gel approaches, has a strong influence on the accuracy and robustness of quantitative proteomics workflows. The major benefit of in-gel procedures is their compatibility with detergents (such as SDS) for protein solubilization. However, SDS-PAGE
    Markus Brosch et al.
    Molecular & cellular proteomics : MCP, 7(5), 962-970 (2008-01-25)
    It is a major challenge to develop effective sequence database search algorithms to translate molecular weight and fragment mass information obtained from tandem mass spectrometry into high quality peptide and protein assignments. We investigated the peptide identification performance of Mascot
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