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Key Documents

SAB2500663

Sigma-Aldrich

Anti-MYB/C-MYB antibody produced in goat

affinity isolated antibody, buffered aqueous solution

Synonyme(s) :

Anti-MYB, Anti-Myeloblastosis viral (v-myb) oncogene homolog, avian, Anti-c-Myb_CDS, Anti-v-myb Myeloblastosis viral oncogene homolog (avian)

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About This Item

Numéro MDL:
MFCD01633889
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

goat

Niveau de qualité

100

Conjugué

unconjugated

Forme d'anticorps

affinity isolated antibody

Type de produit anticorps

primary antibodies

Clone

polyclonal

Forme

buffered aqueous solution

Espèces réactives

human, mouse, rat, canine

Technique(s)

immunohistochemistry: suitable
indirect ELISA: suitable
western blot: suitable

Numéro d'accès UniProt

P10242

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... MYB(4602)

Description générale

Myeloblastosis (MYB) proto-oncogene, transcription factor (MYB) gene codes for a transcriptional activator, Myb-nuclear factor 1 B-type (MYB-NFIB), and is located on human chromosome 6q23.3.

Immunogène

Peptide with sequence C-QRHYNDEDPEKEKR from the internal region of the protein sequence according to NP_005366.2.

Actions biochimiques/physiologiques

Myeloblastosis (MYB) proto-oncogene, transcription factor (MYB) plays a key role in modulating various cellular genes that participates in the proliferation, differentiation, and apoptosis of cells. This protein promotes the development and metastasis of salivary adenoid cystic carcinoma (SACC). MYB plays ah role in initiating and maintaining acute leukemias. It participates in pancreatic cancer, prostate cancer, colorectal cancer, and breast cancer (BC).

Caractéristiques et avantages

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Forme physique

Supplied at 0.5 mg/mL in Tris saline with 0.02% sodium azide and 0.5% bovine serum albumin.

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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Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319

Conseils de prudence

P305 + P351 + P338

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

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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Consulter la Bibliothèque de documents

Ren-Ming Yang et al.
Oncogene, 38(26), 5239-5249 (2019-04-12)
Over 70% of human breast cancers are estrogen receptor-positive (ER+), most of which express MYB. In these and other cell types, the MYB transcription factor regulates the expression of many genes involved in cell proliferation, differentiation, tumorigenesis, and apoptosis. So
Li-Hua Xu et al.
International journal of oncology, 54(5), 1579-1590 (2019-03-22)
The incidence of recurrent t(6;9) translocation of the MYB proto‑oncogene to NFIB (the gene that encodes nuclear factor 1 B‑type) in adenoid cystic carcinoma (ACC) tumour tissues is high. However, MYB [the gene that encodes transcriptional activator Myb (MYB)] overexpression is more common
Eleni M Rettig et al.
The Laryngoscope, 125(9), E292-E299 (2015-05-13)
Salivary gland adenoid cystic carcinoma (ACC) is rare, aggressive, and challenging to treat. Many ACCs have a t(6;9) chromosomal translocation resulting in a MYB-NFIB fusion gene, but the clinical significance is unclear. The purposes of this study were to describe

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