SDHA Recombinant Rabbit mAb (一抗) - WB,IHC-P,IHC-F,IF,Flow-Cyt,ICC/IF,IP | Bioss

Rrmab?兔单抗
2026-05-01~2026-06-30,AB2605
SDHA Recombinant Rabbit mAb (一抗) - WB,IHC-P,IHC-F,IF,Flow-Cyt,ICC/IF,IP | Bioss
货号:bsm-61435R
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概述

产品编号
bsm-61435R
产品类型
重组兔单抗
英文名称
SDHA Recombinant Rabbit mAb
中文名称
琥珀酸脱氢酶复合体亚基A重组兔单抗
英文别名
SDHA_HUMAN; SDHA; Flavoprotein subunit of complex II (Fp); Malate dehydrogenase [quinone] flavoprotein subunit; 1.3.5.1; SDH2; SDHF; CMD1GG; FP; MC2DN1; NDAXOA; PGL5; PPGL5; SDH1; succinate dehydrogenase complex flavoprotein subunit A; succinate dehydrogenase complex, subunit A, flavoprotein (Fp); succinate dehydrogenase complex subunit A, flavoprotein (Fp); succinate dehydrogenase [ubiquinone] flavoprotein subunit; flavoprotein subunit of complex II
抗体来源
Rabbit
免疫原
A synthesized peptide derived from human SDHA: 575-621
亚型
IgG
性状
Liquid
纯化方法
affinity purified by Protein A
克隆类型
Recombinant
克隆号
6A12
理论分子量
73 kDa
检测分子量
68 kDa
储存液
10mM phosphate buffered saline(pH 7.4) with 150mM sodium chloride, 0.05% BSA, 0.02% Proclin300 and 50% glycerol.
SWISS
Gene ID
保存条件
Store at 4℃ for short term. Store at -20℃ for long term. Avoid repeated freeze/thaw cycles.
注意事项
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
背景资料
Flavoprotein (FP) subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone.
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产品应用

应用已检合格种属预测种属推荐稀释比例
WBHuman, Mouse, Rat1:500-2000
IHC-PHuman, Mouse, Rat1:50-200
IHC-FHuman, Mouse, Rat1:50-200
IFHuman, Mouse, Rat1:50-200
Flow-CytHuman, Mouse, Rat1:50-100
ICC/IFHuman, Mouse, Rat1:50-200
IPHuman, Mouse, Rat1:20-50

交叉反应

交叉反应: Human, Mouse, Rat

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靶标

基因名
SDHA
蛋白名
Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial
功能
Defects in SDHA are a cause of mitochondrial complex II deficiency (MT-C2D). A disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations. Clinical features include psychomotor regression in infants, poor growth with lack of speech development, severe spastic quadriplegia, dystonia, progressive leukoencephalopathy, muscle weakness, exercise intolerance, cardiomyopathy. Some patients manifest Leigh syndrome or Kearns-Sayre syndrome.

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