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Rabbit Anti-MT-ND6 antibody
多克隆  |   SKU:bs-22462R

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货号:bs-3351R
¥1280
订购号:bs-22462R
¥1138.00-2900.00
货期:现货
Rabbit Anti-MT-ND6 antibody
反应物种(预测)

Rabbit

产品应用(已验证)

WB

推荐稀释比例

WB=1:500-2000,

研究领域

肿瘤,细胞生物,免疫学,神经生物学,转录调节因子

标签

Array

  • Sample:
    Spleen (Mouse) Lysate at 40 ug
    Spleen (Rat) Lysate at 40 ug
    Primary: Anti-MT-ND6 (bs-22462R) at 1/1000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 24 kD
    Observed band size: 24 kD

产品信息

RRID:RRID
产品名称:Rabbit Anti-MT-ND6 antibody
别名: Mitochondrially encoded NADH dehydrogenase 6; NADH-ubiquinone oxidoreductase chain 6; MT ND6; mtND6; NADH dehydrogenase subunit 6 (complex I); NADH dehydrogenase subunit 6; NADH ubiquinone oxidoreductase chain 6; NADH Ubiquinone Oxidoreductase subunit ND6
中文名称:NADH复合体6抗体
英文名称:Rabbit Anti-MT-ND6 antibody
抗体来源: Rabbit
克隆类型:多克隆
细胞定位:细胞浆
性 状:Liquid
亚 型:IgG
纯化方法:affinity purified by Protein A
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

免疫原信息

免 疫 原:KLH conjugated synthetic peptide derived from mouse MT-ND6
抗原表位:31-130/172
SWISS:P03923
Gene ID :4541
Human Gene ID:4541

产品介绍

NADH Dehydrogenase subunit 6 (MTND6) is 1 of the 7 mitochondrial DNA (mtDNA) encoded subunits (MTND1, MTND2, MTND3, MTND4L, MTND4, MTND5, MTND6) included among the approximately 41 polypeptides of respiratory Complex I. Complex I accepts electrons from NADH, transfers them to ubiquinone (Coenzyme Q10), and uses the energy released to pump protons across the mitochondria inner membrane. MTND6 has been proposed to be a component of the iron-protein fragment.
Function:Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The
Subcellular Location:Mitochondrion membrane; Multi-pass membrane protein (Potential).
DISEASE:Defects in MT-ND6 are a cause of Leber hereditary optic neuropathy (LHON) [MIM:535000]. LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurologic
Similarity:Belongs to the complex I subunit 6 family.
Important Note:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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