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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:
10
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biological source

mouse

Quality Level

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

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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相关内容

A major focus of breast cancer research is to understand the mechanisms responsible for disease progression and drug resistance. Toward that end, it has been found that approximately two thirds of all human breast carcinomas overexpress the Estrogen Receptor α (ERα) protein and it remains the primary pharmacological target for endocrine therapy1,2. The normal cellular function of ERα is as a transcription factor that mediates a wide variety of physiological processes, many of which are dependent upon phosphorylation of the receptor at specific amino acid residues3,4. Indeed, ERα is known to be phosphorylated at a multitude of different sites, yet how these all correlate to disease remains unclear5. Here, we interrogated multiple sites of ERα for phosphorylation status by screening an extensive panel of different breast cancer patient samples and other non-breast cancer tissue microarray (TMA) slide samples to determine their relevance to disease.


The stress protein/chaperone Grp94 counteracts muscle disuse atrophy by stabilizing subsarcolemmal neuronal nitric oxide synthase.
Vitadello, M; Gherardini, J; Gorza, L
Antioxidants & Redox Signaling null
Impact of the phosphatidylinositide 3-kinase signaling pathway on the cardioprotection induced by intermittent hypoxia.
Milano, G; Abruzzo, PM; Bolotta, A; Marini, M; Terraneo, L; Ravara, B; Gorza et al.
Testing null
L Gorza et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 14(3), 461-475 (2000-03-04)
We previously showed that skeletal myocytes of the adult rabbit do not accumulate the endoplasmic reticulum glucose-regulated protein GRP94, neither constitutively nor inducibly, at variance with skeletal myocytes during perinatal development (5). Here we show that C2C12 cells up-regulate GRP94



全球贸易项目编号

货号GTIN
MABT82904055977182842