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Merck
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Fontos dokumentumok

05-807

Sigma-Aldrich

Anti-phospho-CREB (Ser133) Antibody, clone 634-2

clone 634-2, Upstate®, from mouse

Szinonimák:

active transcription factor CREB, cAMP responsive element binding protein 1, cAMP-response element-binding protein-1, transactivator protein

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
12352203
eCl@ss:
32160702
NACRES:
NA.41
klón:
634-2, monoclonal
application:
ICC
IF
WB
faj reaktivitás:
rat, mouse
technika/technikák:
immunocytochemistry: suitable
immunofluorescence: suitable
western blot: suitable
citations:
18

biológiai forrás

mouse

Minőségi szint

antitest forma

purified antibody

antitest terméktípus

primary antibodies

klón

634-2, monoclonal

faj reaktivitás

rat, mouse

gyártó/kereskedő neve

Upstate®

technika/technikák

immunocytochemistry: suitable
immunofluorescence: suitable
western blot: suitable

izotípus

IgG1κ

NCBI elérési szám

UniProt elérési szám

kiszállítva

dry ice

célzott transzláció utáni módosítás

phosphorylation (pSer133)

Géninformáció

human ... CREB1(1385)

Általános leírás

CREB is a β ZIP transcription factor that activates target genes through cAMP response elements. CREB is able to mediate signals from numerous physiological stimuli, resulting in regulation of a broad array of cellular responses. While CREB is expressed in numerous tissues, it plays a large regulatory role in the nervous system. CREB is believed to play a key role in promoting neuronal survival, precursor proliferation, neurite outgrowth and neuronal differentiation in certain neuronal populations. Additionally, CREB signaling is involved in learning and memory in several organisms. CREB is able to selectively activate numerous downstream genes through interactions with different dimerization partners. CREB is activated by phosphorylation at Ser133 by various signaling pathways including Erk, Ca2+ and stress signaling. Some of the kinases involved in phosphorylating CREB at Ser133 are p90RSK, MSK, CaMKIV and MAPKAPK-2.

Egyediség

Broad species cross-reactivity expected, based on sequence homology.
Phospho-CREB (Ser133).

Immunogén

A proprietary immunogen based on the amino acid sequence containing phospho-serine corresponding to residue 133 of human CREB.
Epitope: Ser133

Alkalmazás

Beadlyte Specificity Assay:
1:500 to 1:32,000 dilutions of this lot detected CREB peptide containing phosphoserine 133. The antibody did NOT recognize the nonphosphorylated peptide of the same sequence

Immunofluorescence / Immunocytochemistry:
This antibody has been reported by an independent laboratory to detect phospho-CREB (Ser133) using immunofluorescence.
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Transcription Factors
Use Anti-phospho-CREB (Ser133) Antibody, clone 634-2 (mouse monoclonal antibody) validated in ICC, IF, WB to detect phospho-CREB (Ser133) also known as active transcription factor CREB, cAMP responsive element binding protein 1.

Minőség

Routinely evaluated by western blot on RIPA lysates from forskolin treated rat PC-12 and mouse 3T3/A31 cells.

Western Blot Analysis:
A 1:1,000 to 1:4,000 dilution of this lot detected phospho-CREB (Ser 133) in RIPA lysates from forskolin treated rat PC-12 and mouse 3T3/A31 cells (Figure A).

Cél megnevezése

43 kDa

Fizikai forma

Format: Purified
Protein G Purified
Purified mouse IgG1κ in buffer containing 0.014 M phosphate buffer, pH 7.6, 0.175 M NaCl, 0.07% sodium azide and 30% glycerol. Liquid at -20ºC.

Tárolás és stabilitás

Stable for 1 year at -20°C from date of receipt. For maximum recovery of product, centrifuge the vial prior to removing the cap.

Analízis megjegyzés

Control
Human breast carcinoma, forskolin- and FGF-treated SK-N-MC cell extracts.

Egyéb megjegyzések

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

Jogi információk

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

Jogi nyilatkozat

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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Tárolási osztály kódja

10 - Combustible liquids

WGK

WGK 1


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Dokumentumtár megtekintése

Balapal S Basavarajappa et al.
Hippocampus, 24(7), 808-818 (2014-03-22)
In rodents, many exogenous and endogenous cannabinoids, such as anandamide (AEA) and 2-arachidonyl glycerol (2-AG), have been shown to play an important role in certain hippocampal memory processes. However, the mechanisms by which endogenous AEA regulate this processes are not
A composite element that binds basic helix loop helix and basic leucine zipper transcription factors is important for gonadotropin-releasing hormone regulation of the follicle-stimulating hormone beta gene.
Ciccone, NA; Lacza, CT; Hou, MY; Gregory, SJ; Kam, KY; Xu, S; Kaiser, UB
Molecular Endocrinology null
Marcelo T Marin et al.
The European journal of neuroscience, 30(10), 1931-1940 (2009-11-17)
Learned associations are hypothesized to develop between drug effects and contextual stimuli during repeated drug administration to produce context-specific sensitization that is expressed only in the drug-associated environment and not in a non-drug-paired environment. The neuroadaptations that mediate such context-specific
Yueh-Ting Tsai et al.
Iranian journal of basic medical sciences, 27(6), 706-716 (2024-04-22)
This study assessed the effects of electroacupuncture (EA) stimulation at different frequencies at the Dazhui and Baihui acupoints in the subacute phase after transient global cerebral ischemia (GCI). Rats were subjected to GCI for 25 min, followed by reperfusion for
Rodrigo Molini Leão et al.
Pharmacology, biochemistry, and behavior, 101(3), 434-442 (2012-02-15)
Experimental evidence shows that exposure to stress engenders behavioral sensitization and increases drug-seeking and leads to intense drug taking. However the molecular mechanisms involved in these processes is not well known yet. The present experiments examined the effects of exposure

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