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Merck
모든 사진(2)

주요 문서

E2645

Sigma-Aldrich

Epidermal Growth Factor Receptor human

lyophilized powder, ≥15,000 units/mg protein (Bradford)

동의어(들):

ERBB, ErbB1, HER1, EGFR

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크기 선택

500 UNITS
₩1,144,514

₩1,144,514


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

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500 UNITS
₩1,144,514

About This Item

MDL number:
UNSPSC 코드:
12352202
NACRES:
NA.32

₩1,144,514


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

생물학적 소스

human

Quality Level

양식

lyophilized powder

효능

>15000.00 units/mg

특이 활성도

≥15,000 units/mg protein (Bradford)

분자량

~170 kDa

포장

pkg of 500UN

저장 조건

avoid repeated freeze/thaw cycles

기술

cell based assay: suitable

색상

white

solubility

glycerol: 10%, clear to slightly hazy, colorless

UniProt 수납 번호

배송 상태

dry ice

저장 온도

−20°C

유전자 정보

human ... EGFR(1956)

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일반 설명

Research area: Cell signaling

Epidermal growth factor receptor (EGFR) belongs to a family of cell surface receptors called receptor tyrosine kinases (RTKs) and is also the most studied member of this family. The EGFR is encoded by the ErbB gene, mapped to chromosome 7 q22.[1] These receptors are attached to the cytoplasmic membrane and [2] consist of an ectodomain (ECD), comprising of four subdomains called DI-DIV, a hydrophobic transmembrane domain, and an intracytoplasmic tyrosine kinase domain.

생화학적/생리학적 작용

170 kDa glycoprotein having EGF-activated protein tyrosine kinase activity; high levels of EGFR are expressed in approximately one third of human epithelial tumors, and in the cancers of the bladder, breast or lung that have poor clinical prognosis.
EGF exerts its actions by binding to the EGF receptor (EGFR), a 170 kDa glycoprotein having EGF-activated protein tyrosine kinase activity. Even in the absence of EGF-like ligands, EGFR can participate in cellular responses elicited by several other stimuli. High levels of EGFR are expressed in approximately one third of human epithelial tumors, and in the cancers of the bladder, breast or lung that have poor clinical prognosis, hence the interest in targeting EGFR.
Epidermal growth factor receptor (EGFR) has an essential role in normal developmental processes, and is mutated in multiple cancers.[3] It is involved in the pathogenesis of epidermoid tumors, and thus, has extreme importance as a cancer therapeutic target.[4] Gefitinib (GEF) and erlotinib act as EGFR inhibitors, and induce apoptosis in non-small cell lung cancer (NSCLC) cells.[5] A truncated isoform, called EGFRvIII is linked to multiple cases of head and neck squamous cell carcinoma (HNSCC). In ∼40% of glioblastoma multiforme (GBM), this gene is amplified.[6]

단위 정의

One unit (U) of the enzyme is defined as the amount needed to incorporate 1 pmol of phosphate into the substrate (KVEKIGEGTYGVVYK: 6 - 20 residue of p34cdc2) in 1 minute.

물리적 형태

Lyophilized from a solution in 50 mM HEPES, pH 7.6, 150 mM NaCl, 0.05% Triton X-100, 1 mM dithiothreitol, and 10% trehalose.

제조 메모

Affinity purified from human carcinoma A431 cells.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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이미 열람한 고객

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A comprehensive pathway map of epidermal growth factor receptor signaling
Oda K, et al.
Molecular Systems Biology (2005)
The Epidermal Growth Factor Receptor Pathway: A Model for Targeted Therapy
Scaltriti M and Baselga J
Journal of Separation Science null
EGFR/MDM2 signaling promotes NF-?B activation via PPAR? degradation
Xu Y, et al.
Carcinogenesis, 37(2), 215-222 (2016)
Epidermal Growth Factor Receptor Cell Proliferation Signaling Pathways
Wee P and Wang Z
Cancers, 9(5), 52-52 (2017)
Qian Gou et al.
Oncogene, 39(25), 4844-4853 (2020-05-23)
In response to nutrient deficiency, autophagy degrades cytoplasmic materials and organelles in lysosomes, which is nutrient recycling, whereas activation of EGFR mediates autophagy suppression in response to growth factors. It is unclear whether PPARδ could be the regulator of autophagy

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