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M8770

Sigma-Aldrich

Anti-Mouse IgG1 (heavy chain specific) antibody produced in goat

affinity isolated antibody, lyophilized powder

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Synonym(s):
Anti-Mouse Igg1, Heavy Chain Specific Secondary Antibody, Heavy Chain Specific Secondary Antibody - Anti-Mouse IgG1 (heavy chain specific) antibody produced in goat
MDL number:
NACRES:
NA.46

biological source

goat

Quality Level

200
300

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

lyophilized powder

technique(s)

Ouchterlony double diffusion: suitable

storage temp.

2-8°C

target post-translational modification

unmodified

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This Item
M4280M4155I0884
technique(s)

Ouchterlony double diffusion: suitable

technique(s)

indirect ELISA: 1:20,000

technique(s)

Ouchterlony double diffusion: suitable, indirect ELISA: 1:15,000

technique(s)

Ouchterlony double diffusion: suitable

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

form

lyophilized powder

form

-

form

-

form

lyophilized powder

clone

polyclonal

clone

polyclonal

clone

polyclonal

clone

polyclonal

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General description

Immunoglobulin IgG is a glycoprotein antibody with two light chains and a pair of identical heavy chains.

Immunogen

Mouse IgG1 (myeloma protein)

Application

Anti-Mouse IgG1 (heavy chain specific) antibody is suitable for use in immunoelectrophoresis and Ouchterlony double diffusion. The antibody may also be used in immunoblot .
Anti-Mouse IgG1 (heavy chain specific) antibody produced in goat has been used in immunohistochemistry and enzyme-linked immunosorbent assay (ELISA)

Biochem/physiol Actions

Digestion of IgG by papain results in the generation of fragment antigen-binding (Fab). Pepsin digestion of IgG results in fragment crystallizable (fc). IgG1 is most abundant of IgG types and its deficiency results in hypogammaglobulinemia.

Physical form

Lyophilized from 0.01 M phosphate buffered saline, pH 7.2.

Reconstitution

Reconstitute with 0.135 M sodium chloride.

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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A H Schrijvers et al.
Cancer research, 53(18), 4383-4390 (1993-09-15)
Using viable cells of a human head and neck squamous cell carcinoma (HNSCC) cell line as immunogen, we developed monoclonal antibody (MAb) U36. Immunohistochemical examination revealed distinct surface labeling of MAb U36 with normal human squamous epithelium and squamous cell
The combined effect of mesenchymal stem cells and resveratrol on type 1 diabetic neuropathy
Wang C, et al.
Experimental and Therapeutic Medicine, 17(5), 3555-3563 (2019)
J Pass et al.
Scandinavian journal of immunology, 58(3), 298-305 (2003-09-03)
The urokinase receptor (uPAR) is a glycolipid-anchored cell surface glycoprotein that plays a central role in extracellular proteolysis during tissue remodeling processes including cancer invasion. Furthermore, uPAR is found on the surface of both dendritic cells (DCs) and T cells
Louis-P Vézina et al.
Plant biotechnology journal, 7(5), 442-455 (2009-05-09)
Plant-based transient expression is potentially the most rapid and cost-efficient system for the production of recombinant pharmaceutical proteins, but safety concerns associated with plant-specific N-glycosylation have hampered its adoption as a commercial production system. In this article, we describe an
Min-Kyung Sung et al.
Molecular biology of the cell, 27(17), 2642-2652 (2016-07-08)
Ribosome assembly is an essential process that consumes prodigious quantities of cellular resources. Ribosomal proteins cannot be overproduced in Saccharomyces cerevisiae because the excess proteins are rapidly degraded. However, the responsible quality control (QC) mechanisms remain poorly characterized. Here we

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