MABS2036M

Anti-Cytochrome b Antibody, clone 5B3-6E3

clone 5B3-6E3, from mouse

• 别名: Cytochrome b (UniProt: P00156, also known as Complex III subunit 3, Complex III subunit III, Cytochrome b-c1 complex subunit 3, Ubiquinol-cytochrome-c reductase complex cytochrome b subunit
• 分類程式碼代碼: 12352203
• eCl@ss: 32160702
• NACRES: NA.41

属性

• 生物源: mouse
• 品質等級: 100
• 抗體表格: purified immunoglobulin
• 抗體產品種類: primary antibodies
• 無性繁殖: 5B3-6E3, monoclonal
• 物種活性: human
• 包裝: antibody small pack of 25 μg
• 技術: western blot: suitable
• 同型: IgG2bκ
• NCBI登錄號: YP_003024038.1
• UniProt登錄號: P00156
• 目標翻譯後修改: unmodified
• 基因資訊: human ... MT-CYB(4519)

说明

一般說明

Cytochrome b (UniProt: P00156; also known as Complex III subunit 3, Complex III subunit III, Cytochrome b-c1 complex subunit 3, Ubiquinol-cytochrome-c reductase complex cytochrome b subunit) is encoded by the MT-CYB (also known as COB, CYTB, MTCYB) gene (Gene ID: 4519) in human. Cytochrome b is a mitochondrial inner membrane protein that is a component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex). It is a part of the mitochondrial respiratory chain. The b-c1 complex mediates electron transfer from ubiquinol to cytochrome c and contributes to the generation of a proton gradient across the mitochondrial membrane, which is used for ATP synthesis. The MT-CYB gene is a good phylogenetic marker. Defects in MT-CYB gene are a rare cause of mitochondrial dysfunction underlying different myopathies, which include mitochondrial encephalomyopathy, hypertrophic cardiomyopathy, and sporadic mitochondrial myopathy. Some cases of Leber hereditary optic neuropathy (LHON) are also linked to defects in MT-CYB gene, which result in acute or subacute loss of central vision, due to optic nerve dysfunction.

特異性

Clone 5B3-6E3 detects cytochrome b in human mitochondria. It targets an epitope within the N-terminal region.

免疫原

Epitope: N-terminus

KLH-conjugated Synthetic peptide corresponding to the N-terminus of human cytochrome b.

應用

Anti-Cytochrome b, clone 5B3-6E3, Cat. No. MABS2036, is a mouse monoclonal antibody that detects Complex III Cytochrome b and has been tested for use in Western Blotting.

Research Category
Signaling

Western Blotting Analysis: 0.1 µg/mL from a representative lot detected Cytochrome b in mitochondria from human neonatal dermal fibroblasts and mitochondria from human neonatal dermal fibroblasts depleted of mtDNA. (Courtesy of Michael F. Marusich, Ph.D., mAbDx, Inc., Eugene, OR USA)

品質

Evaluated by Western Blotting in Mitochondria from human neonatal dermal fibroblasts and mitochondria from human neonatal dermal fibroblasts depleted of mtDNA.

Western Blotting Analysis: 0.1 µg/mL of this antibody detected Cytochrome b in Mitochondria from human neonatal dermal fibroblasts and mitochondria from human neonatal dermal fibroblasts depleted of mtDNA.

標靶描述

~28 kDa observed; 42.72 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

外觀

Protein L

Format: Purified

Purified mouse monoclonal antibody IgG2b in buffer containing HEPES-Buffered Saline (150 mM NaCl, 15 mM HEPES, pH 7.2) with 0.02% sodium azide.

儲存和穩定性

Stable for 1 year at 2-8°C from date of receipt.

其他說明

Concentration: Please refer to lot specific datasheet.

免責聲明

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.

安全信息

• 儲存類別代碼: 12 - Non Combustible Liquids
• 水污染物質分類（WGK）: WGK 1
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable