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Key Documents

MABC521

Sigma-Aldrich

Anti-XBP1s Antibody, clone 143F (active form)

clone 143F, from mouse

Synonim(y):

X-box-binding protein 1, XBP-1, Tax-responsive element-binding protein 5

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About This Item

Kod UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

pochodzenie biologiczne

mouse

Poziom jakości

forma przeciwciała

purified immunoglobulin

rodzaj przeciwciała

primary antibodies

klon

143F, monoclonal

reaktywność gatunkowa

human

metody

immunohistochemistry: suitable
western blot: suitable

izotyp

IgG2aκ

numer dostępu NCBI

numer dostępu UniProt

Warunki transportu

wet ice

docelowa modyfikacja potranslacyjna

unmodified

informacje o genach

human ... XBP1(7494)

Opis ogólny

XBP-1, also known as X-box-binding protein 1 or Tax-responsive element-binding protein 5, and encoded by the gene XBP1/TREB5/XBP2, is a transcription factor essential for hepatocyte growth, the differentiation of plasma cells, immunoglobulin secretion, and the unfolded protein response (UPR). XBP-1 also acts during endoplasmic reticulum stress (ER) by activating unfolded protein response (UPR) target genes via direct binding to the UPR element (UPRE). XBP-1 binds DNA preferentially at CRE-like elements but also to some TPA response elements (TRE). XBP-1 is expressed in the nucleus. Defects in XBP-1 may be associated with Major affective disorder 7 (MAFD7) a major psychiatric disorder that is characterized by severe mood swings, with fluctuation between two abnormal mood states (manic or major depressive episode). Mania is accompanied by symptoms of euphoria, irritability, or excitation, whereas depression is associated with low mood and decreased motivation and energy.

Immunogen

Epitope: C-terminus
GST-tagged recombinant protein corresponding to the C-terminus of human XBP-1S, clone 143F (active form).

Zastosowanie

Anti-XBP1s Antibody, clone 143F (active form) is an antibody against XBP1s for use in IHC & western blotting.
Research Category
Apoptosis & Cancer
Research Sub Category
Apoptosis - Additional
Western Blotting Analyis: A representative lot from an independent laboratory detected XBP-1S, clone 143F (active form) in SK-MM-2, KARPAS 620, NCI-H929, and LP-1 cell lysates (Maestre, L., et al. (2009). Haematologica. 94(3):419-422.).

Immunohistochemistry Analysis: A representative lot from an independent laboratory detected XBP-1S, clone 143F (active form) in human tonsil and lymphoplasmacytic cells (Maestre, L., et al. (2009). Haematologica. 94(3):419-422.).

Jakość

Evaluated by Immunohistochemistry in human skin tissues.

Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected XBP-1S, clone 143F (active form) in human skin tissues.

Opis wartości docelowych

29 kDa calculated

Postać fizyczna

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG2aκ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Przechowywanie i stabilność

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

Inne uwagi

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Oświadczenie o zrzeczeniu się odpowiedzialności

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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Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Clara Lucía León-Annicchiarico et al.
The FEBS journal, 282(18), 3647-3658 (2015-07-15)
Altered metabolism is a hallmark of cancer that opens new therapeutic possibilities. 2-deoxyglucose (2-DG) is a non-metabolizable glucose analog tested in clinical trials and is frequently used in experimental settings to mimic glucose starvation. However, in the present study, conducted

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