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Merck
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Fontos dokumentumok

PLA0001

Sigma-Aldrich

Anti-c-Myc Tag Antibody

rabbit polyclonal

Szinonimák:

MRTL, MYCC, avian myelocytomatosis viral oncogene homolog, bHLHe39, c-Myc, class E basic helix-loop-helix protein 39, myc-related translation/localization regulatory factor, proto-oncogene c-Myc, transcription factor p64, v-myc myelocytomatosis viral oncogene homolog

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
12352203
NACRES:
NA.41
faj reaktivitás:
human
application:
ELISA
ICC
IP
WB
technika/technikák:
ELISA: 1:1,000- 1:30,000
ELISA: 1:100- 1:500 (for coating plates)
immunocytochemistry: 1:100-1:400
immunoprecipitation (IP): 1- 4 μg/mg
western blot: 1:1,000- 1:30,000
citations:
19

Terméknév

Rabbit anti-c-myc Antibody, Affinity Purified, Powered by Bethyl Laboratories, Inc.

biológiai forrás

rabbit

Minőségi szint

antitest forma

affinity purified immunoglobulin

antitest terméktípus

primary antibodies

grade

Powered by Bethyl Laboratories, Inc.

faj reaktivitás

human

technika/technikák

ELISA: 1:1,000- 1:30,000
ELISA: 1:100- 1:500 (for coating plates)
immunocytochemistry: 1:100-1:400
immunoprecipitation (IP): 1- 4 μg/mg
western blot: 1:1,000- 1:30,000

elérési szám

NP_002458.2

kiszállítva

wet ice

tárolási hőmérséklet

2-8°C

célzott transzláció utáni módosítás

unmodified

Géninformáció

rabbit ... c-myc(4609)

Immunogén

Rabbits were immunized with a synthetic peptide representing amino acid residues 410—419 (EQKLISEEDL) of human myc conjugated to KLH. Antibody was isolated by affinity chromatography using the peptide immobilized on solid support.

Fizikai forma

Phosphate Buffered Saline (PBS) containing 0.09% Sodium Azide

Egyéb megjegyzések

The c-myc epitope tag is a commonly used epitope tag engineered onto the N- or C- terminus of a protein of interest so that the tagged protein can be analyzed and visualized using immunochemical methods. The recognized c-myc epitope represents amino acid residues 410-419, EQKLISEEDL, of human c-myc.

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

12 - Non Combustible Liquids

WGK

nwg

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable


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Analitikai tanúsítványok (COA)

Lot/Batch Number

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Dokumentumtár megtekintése

Charles Campbell et al.
Journal of cell science, 129(20), 3832-3844 (2016-09-17)
Sonic Hedgehog (Shh) is a secreted morphogen that is an essential regulator of patterning and growth. The Shh full-length protein undergoes autocleavage in the endoplasmic reticulum to generate the biologically active N-terminal fragment (ShhN), which is destined for secretion. We
Jana Kralovicova et al.
Cancers, 12(7) (2020-07-16)
U2AF65 (U2AF2) and PUF60 (PUF60) are splicing factors important for recruitment of the U2 small nuclear ribonucleoprotein to lariat branch points and selection of 3' splice sites (3'ss). Both proteins preferentially bind uridine-rich sequences upstream of 3'ss via their RNA
Shuo Yang et al.
Developmental biology, 495, 35-41 (2022-12-18)
Cell fate specification is essential for every major event of embryogenesis, and subsequent cell maturation ensures individual cell types acquire specialized functions. The mechanisms that regulate cell fate specification have been studied exhaustively, and each technological advance in developmental biology
Javier Vázquez-Marín et al.
Development (Cambridge, England), 146(13) (2019-05-31)
Yap1/Taz are well-known Hippo effectors triggering complex transcriptional programs controlling growth, survival and cancer progression. Here, we describe yap1b, a new Yap1/Taz family member with a unique transcriptional activation domain that cannot be phosphorylated by Src/Yes kinases. We show that
Reuben J Pengelly et al.
Nucleic acids research, 50(10), 5493-5512 (2022-04-28)
Auxilliary splicing sequences in exons, known as enhancers (ESEs) and silencers (ESSs), have been subject to strong selection pressures at the RNA and protein level. The protein component of this splicing code is substantial, recently estimated at ∼50% of the

Tudóscsoportunk valamennyi kutatási területen rendelkezik tapasztalattal, beleértve az élettudományt, az anyagtudományt, a kémiai szintézist, a kromatográfiát, az analitikát és még sok más területet.

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