SLC25A46 Antibody
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货号:CSB-PA856895LA01HU
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规格:¥440
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促销:
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图片:
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Western blot
All lanes: SLC25A46 antibody at 6µg/ml
Lane 1: Mouse brain tissue
Lane 2: Jurkat whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 47, 31, 38 kDa
Observed band size: 47 kDa -
Immunofluorescent analysis of Hela cells using CSB-PA856895LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) SLC25A46 Polyclonal antibody
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Uniprot No.:Q96AG3
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基因名:SLC25A46
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别名:SLC25A46; TB1; Solute carrier family 25 member 46
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宿主:Rabbit
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反应种属:Human, Mouse
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免疫原:Recombinant Human Solute carrier family 25 member 46 protein (1-102AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,SLC25A46 Antibody (CSB-PA856895LA01HU),的标记方式是Non-conjugated。对于SLC25A46 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB, IF
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推荐稀释比:
Application Recommended Dilution WB 1:1000-1:5000 IF 1:50-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能:May play a role in mitochondrial dynamics by controlling mitochondrial membrane fission.
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基因功能参考文献:
- This study reported a novel variant (p.Trp160Ser) in SLC25A46 and we broaden the phenotypic spectrum associated with mutations in SLC25A46. PMID: 28558379
- This study identified of a homozygous missense mutation c.1022T>C and a homozygous genomic deletion involving exon 1 in SLC25A46 encoding a mitochondrial protein leading to lethal pontocerebellar hypoplasia with apnoea and profound weakness. PMID: 27543974
- These results show that SLC25A46 plays a role in a mitochondrial/endoplasmic reticulum pathway that facilitates lipid transfer, and link altered mitochondrial dynamics to early-onset neurodegenerative disease and cell fate decisions. PMID: 27390132
- SLC25A46 is selectively degraded from the outer membrane independently of mitophagy and apoptosis, providing a framework for mechanistic studies in the proteolysis of outer membrane proteins PMID: 28057766
- we showed that the Slc25a46 disruption caused a fusion/fission imbalance and an abnormal mitochondrial architecture that disturbed mitochondrial metabolism. These data extended the range of phenotypes associated with Slc25a46 dysfunction. Moreover, this Slc25a46 knock-out mouse model should be useful to further elucidate the role of SLC25A46 in mitochondrial dynamics PMID: 28376083
- Our mutant mice provide a valid model for understanding the mechanistic basis of the complex SLC25A46-mediated pathologies, as well as for screening potential therapeutic interventions. PMID: 28376086
- The rs10056340 single nucleotide polymorphism was significantly associated with atopic dermatitis. PMID: 26464032
- Data indicate four families with recessive mutations in solute carrier family 25 member 46 protein (SLC25A46). PMID: 26168012
- Rs17132261 was associated with left ventricular hypertrophy in type 2 diabetic patients. PMID: 23879873
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相关疾病:Neuropathy, hereditary motor and sensory, 6B (HMSN6B)
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亚细胞定位:Mitochondrion outer membrane; Multi-pass membrane protein.
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蛋白家族:Mitochondrial carrier (TC 2.A.29) family
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数据库链接:
HGNC: 25198
OMIM: 610826
KEGG: hsa:91137
STRING: 9606.ENSP00000348211
UniGene: Hs.75639
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