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Key Documents

PLA0001

Sigma-Aldrich

Rabbit anti-c-myc Antibody, Affinity Purified

Powered by Bethyl Laboratories, Inc.

Synonyme(s) :

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

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About This Item

Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Niveau de qualité

100

Forme d'anticorps

affinity purified immunoglobulin

Type de produit anticorps

primary antibodies

Qualité

Powered by Bethyl Laboratories, Inc.

Espèces réactives

human

Technique(s)

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

Numéro d'accès

NP_002458.2

Conditions d'expédition

wet ice

Température de stockage

2-8°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

rabbit ... c-myc(4609)

Immunogène

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.

Forme physique

Phosphate Buffered Saline (PBS) containing 0.09% Sodium Azide

Autres remarques

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.

Clause de non-responsabilité

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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Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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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
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
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
Duncan G Ithinji et al.
NPJ vaccines, 7(1), 166-166 (2022-12-18)
Experimental vaccines for the deadly zoonotic Nipah (NiV), Hendra (HeV), and Ebola (EBOV) viruses have focused on targeting individual viruses, although their geographical and bat reservoir host overlaps warrant creation of multivalent vaccines. Here we explored whether replication-incompetent pseudotyped vesicular
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