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C4733

Sigma-Aldrich

BID, Caspase-8-cleaved from mouse

≥95% (SDS-PAGE), recombinant, expressed in E. coli, buffered aqueous solution

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About This Item

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

Pricing and availability is not currently available.

recombinant

expressed in E. coli

Quality Level

assay

≥95% (SDS-PAGE)

form

buffered aqueous solution

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

Gene Information

mouse ... Bid(12122)

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This Item
C1099AB10002C1224
assay

≥95% (SDS-PAGE)

assay

≥90% (SDS-PAGE)

assay

-

assay

≥85% (SDS-PAGE)

recombinant

expressed in E. coli

recombinant

expressed in E. coli (C-terminal histidine tagged)

recombinant

-

recombinant

expressed in E. coli (C-terminal histidine-tagged)

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

200

form

buffered aqueous solution

form

buffered aqueous solution

form

-

form

buffered aqueous glycerol solution

shipped in

dry ice

shipped in

dry ice

shipped in

wet ice

shipped in

dry ice

UniProt accession no.

P70444

UniProt accession no.

Q14790

UniProt accession no.

P70444

UniProt accession no.

P42574

General description

Mouse BID cleaved with caspase-8 generates the amino-terminal fragment (amino acids 1-59, 7 kDa) and the carboxy-terminal fragment (amino acids 60-195, 15 kDa). On size exclusion chromatography cleaved BID elutes at 27 kDa indicating that the fragments remain associated.

Biochem/physiol Actions

Caspase-8-cleaved BID relocates from the cytosol to the outer mitochondrial membrane where its interaction with Bak alters mitochondrial membrane permeability.

Physical form

0.2 μm filtered solution in 25 mM HEPES, pH 7.5, and 0.1 M KCl.

Analysis Note

Measured by its ability to induce cytochrome c release from isolated mouse liver mitochondria.

Storage Class

10 - Combustible liquids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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Sharma, N; Arias, EB; Sequea, DA; Cartee, GD
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The Rab-GTPase-activating protein TBC1D1 regulates skeletal muscle glucose metabolism.
Szekeres, F; Chadt, A; Tom, RZ; Deshmukh, AS; Chibalin, AV; Bjornholm, M; Al-Hasani, H; Zierath, JR
American Journal of Physiology. Endocrinology and Metabolism null
Roberto A Gulli et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 303(10), R1062-R1070 (2012-10-12)
High-fat (HF) diets impair skeletal muscle response to the insulin-sensitizing adipokine adiponectin (Ad) in rodents, preceding the development of insulin resistance. Skeletal muscle insulin response in HF-fed rats can be restored with chronic exercise; whether recovery of skeletal muscle Ad
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The Rab GTPase activating protein known as Akt substrate of 160 kDa (AS160 or TBC1D4) regulates insulin-stimulated glucose uptake in skeletal muscle, the heart, and white adipose tissue (WAT). A novel rat AS160-knockout (AS160-KO) was created with CRISPR/Cas9 technology. Because

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