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Merck
CN

MABT829

Anti-GRP94 Antibody, clone 3C4

clone 3C4, from mouse

别名:

Endoplasmin, 94 kDa glucose-regulated protein, GRP-94, Heat shock protein 90 kDa beta member 1, GRP94

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
3C4, monoclonal
Application:
ICC, IF, IHC, IP, WB
Citations:
5
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biological source

mouse

conjugate

unconjugated

antibody form

purified antibody

antibody product type

primary antibodies

clone

3C4, monoclonal

species reactivity

goat, mouse, rabbit, human

technique(s)

immunocytochemistry: suitable, immunofluorescence: suitable, immunohistochemistry: suitable, immunoprecipitation (IP): suitable, western blot: suitable

isotype

IgG1κ

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Quality Level

Gene Information

human ... HSP90B1(7184)

General description

Endoplasmin (UniProt P14625; also known as 94 kDa glucose-regulated protein, Endothelial cell (HBMEC) glycoprotein, Epididymis luminal protein 35, Epididymis secretory sperm binding protein Li 125m, gp96 homolog, GRP-94, Heat shock protein 90 kDa beta member 1, Stress-inducible tumor rejection antigen gp96, Tumor rejection antigen 1) is encoded by the HSP90B1 (also known as ECGP, GP96, GRP94, HEL35; HEL-S-125m, TRA1) gene (Gene ID 7184) in human. The endoplasmic reticulum (ER) chaperone Grp94 mediates the cell surface export of molecules involved in the native immune response, mesoderm induction, muscle development, cytoprotection against oxidative stress, and calcium homeostasis. Src family tyrosine kinase Fyn-catalyzed Grp94 phosphorylation is reported to be essential for Grp94 export from ER to the Golgi apparatus in the early phase of myoblast differentiation.
~94/110 kDa observed

Immunogen

Epitope: N-terminal half
His-tagged recombinant protein corresponding to the N-terminal of rabbit GRP94.

Application

Anti-GRP94 Antibody, clone 3C4 is an antibody against GRP94 for use in Western Blotting, Immunofluorescence, Immunohistochemistry, Immunoprecipitation, Immunocytochemistry.
Research Category
Cell Structure
Research Sub Category
Adhesion (CAMs)
Western Blotting Analysis: 0.5 µg/mL from a representative lot detected GRP94 in 10 µg of mouse liver and human heart tissue lysate.
Immunofluorescence Analysis: Representative lots detected GRP94 immunoreactivity in rabbit and goat ventricular myocardium sections (Vitadello, M., et al. (1998). Biochem J. 332 ( Pt 2):351-359; Vitadello, M., et al. (2001). Circulation. 103(17):2201-2206)
Immunohistochemistry Analysis: A representative lot detected GRP94 immunoreactivity in fibrillating goat atria (Vitadello, M., et al. (2001). Circulation. 103(17):2201-2206)
Western Blotting Analysis: Representative lots detected GRP94 in atrial myocytes from vairous species, including murine (Milano, G., et al. (2013). PLoS One. 8(10):e76659), goat and human (Vitadello, M., et al. (2001). Circulation. 103(17):2201-2206), and rabbit (Vitadello, M., et al. (1998). Biochem J. 332 ( Pt 2):351-359).
Immunoprecipitation Analysis: A representative lot co-immunoprecipitated nNOS with GRP94 from chemically cross-linked C2C12 murine myoblasts in either proliferating or differentiating cultures (Vitadello, M., et al. (2014). Antioxid Redox Signal. 20(16):2479-2476).
Immunocytochemistry Analysis: A representative lot detected GRP94 immunoreactivity in murine C2C12 skeletal myoblasts as well as primary skeletal myocytes from new born mice (Gorza, L., and Vitadello, M. (2000). FASEB J. 14(3):461-475).

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of receipt.

Analysis Note

Evaluated by Western Blotting in murine myoblast C2C12 cell lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected GRP94 in 10 µg of murine myoblast C2C12 cell lysate.

Other Notes

Concentration: Please refer to lot specific datasheet.

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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存储类别

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Sofia E Gomes et al.
PloS one, 13(1), e0191607-e0191607 (2018-01-24)
MicroRNAs (miRNAs) regulate a wide variety of biological processes, including tumourigenesis. Altered miRNA expression is associated with deregulation of signalling pathways, which in turn cause abnormal cell growth and de-differentiation, contributing to cancer. miR-143 and miR-145 are anti-tumourigenic and influence
Maurizio Vitadello et al.
Arthritis research & therapy, 12(2), R52-R52 (2010-03-26)
The endoplasmic reticulum (ER) stress-response, evoked in mice by the overexpression of class I major histocompatibility complex antigen (MHC-I), was proposed as a major mechanism responsible for skeletal muscle damage and dysfunction in autoimmune myositis. The present study was undertaken

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