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Merck

SRP6265

Sigma-Aldrich

HMGB1/HMG1 human

recombinant, expressed in HEK 293 cells, ≥95% (SDS-PAGE)

Synonym(e):

HMG1, HMG3, HMGB1, SBP-1

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About This Item

UNSPSC-Code:
12352200
NACRES:
NA.32

Biologische Quelle

human

Rekombinant

expressed in HEK 293 cells

Markierung

6-His tagged (C-terminus)

Assay

≥95% (SDS-PAGE)

Form

lyophilized powder

Wirksamkeit

0.22 μg/mL

Mol-Gew.

calculated mol wt 25.7 kDa
observed mol wt 28 kDa (DTT-reduced. Protein migrates due to glycosylation. Phe17 is the predicted N-terminus.)
observed mol wt 32 kDa

Verpackung

pkg of 10 μg

Verunreinigungen

<1 EU/μg endotoxin (LAL test)

UniProt-Hinterlegungsnummer

Versandbedingung

wet ice

Lagertemp.

−20°C

Angaben zum Gen

human ... HMGB1(3146)

Allgemeine Beschreibung

High-mobility group protein B1 (HMGB1), also known as high-mobility group protein 1 (HMG-1) and amphoterin, is a member of the HMGB family consisting of three members, HMGB1, HMGB2 and HMGB3. HMGB1 is a non-histone architectural chromosomal protein ubiquitously present in all vertebrate nuclei and binds double-stranded DNA without sequence specificity. However, it can shuttle between the nucleus and cytoplasm. The protein is secreted by activated monocytes and macrophages. HMGB1 is from the high mobility group protein super family. The gene is mapped to human chromosome 13q12.

Anwendung

HMGB1 (high-mobility group protein B1) has been used to identify factors masking HMGB1 in human serum and plasma. It has been used to study HMGB1-mediated growth and motility in papillary thyroid cancer cells.
HMGB1/HMG1 human has been used as a positive control to analyse the expression of purified HMGB1 gene.

Biochem./physiol. Wirkung

In the nucleus, HMGB1 (high-mobility group protein B1) works as a nucleosome stabilizer and transcriptional regulator. It also exhibits chaperone-like activity and suppresses aggregation of polyglutamine. It is also involved in inflammation and autophagy. HMGB1 can interacts with toll-like receptor (TLR) 2 and 4, interleukin-1β, chemokine (C-X-C motif) ligand 12 (CXCL12) and pathogen-associated molecular pattern (PAMP) molecules. It also works as a damage-associated molecular pattern molecule (DAMP). The mechanism of inflammation and damage is binding to TLR4, which mediates HMGB1-dependent activation of macrophage cytokine release. This positions HMGB1 at the intersection of sterile and infectious inflammatory responses. HMGB1 has been studied as a DNA vaccine adjuvant and a target for cancer therapy. In presence of Epstein-Barr virus (EBV) infection, HMGB1 is upregulated and is responsible for the proliferation of human nasopharyngeal carcinoma cells. It is involved in cancer cell migration and invasion.

Physikalische Form

Lyophilized from 0.22 μm filtered solution in PBS. Generally 5-8% Mannitol or trehalose is added as a protectant before lyophilization.

Rekonstituierung

Centrifuge the vial prior to opening. Reconstitute in sterile PBS, pH 7.4 to a concentration of 50 μg/mL. Do not vortex. This solution can be stored at 2-8°C for up to 1 month. For extended storage, it is recommended to store at -20°C.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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High mobility group box 1 (HMGB1) acts as an ?alarmin? to promote acute myeloid leukaemia progression.
Yasinska I M, et al.
Oncoimmunology, 7(6), e1438109-e1438109 (2018)
Factors masking HMGB1 in human serum and plasma.
Urbonaviciute V
Journal of Leukocyte Biology, 81, 67-74 (2007)
HMGB1 interacts differentially with members of the Rel family of transcription factors.
Agresti A
Biochemical and Biophysical Research Communications, 302, 421-426 (2003)
N-linked glycosylation plays a crucial role in the secretion of HMGB1.
Kim YH
Journal of Cell Science, 129, 29-38 (2016)
Inna M Yasinska et al.
Oncoimmunology, 7(6), e1438109-e1438109 (2018-06-07)
High mobility group box 1 (HMGB1) is a non-histone protein localised in the cell nucleus, where it interacts with DNA and promotes nuclear transcription events. HMGB1 levels are elevated during acute myeloid leukaemia (AML) progression followed by participation of this

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