SLC25A12 Antibody
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货号:CSB-PA021478LA01HU
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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
Positive WB detected in: HEK293 whole cell lysate, Rat heart tissue, Rat kidney tissue, Mouse kidney tissue, Mouse heart tissue
All lanes: SLC25A12 antibody at 3µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 75, 63 kDa
Observed band size: 75 kDa -
Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA021478LA01HU at dilution of 1:100
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Immunohistochemistry of paraffin-embedded human pancreatic cancer using CSB-PA021478LA01HU at dilution of 1:100
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) SLC25A12 Polyclonal antibody
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Uniprot No.:O75746
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基因名:SLC25A12
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别名:SLC25A12; ARALAR1; Calcium-binding mitochondrial carrier protein Aralar1; Mitochondrial aspartate glutamate carrier 1; Solute carrier family 25 member 12
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宿主:Rabbit
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反应种属:Human, Rat, Mouse
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免疫原:Recombinant Human Calcium-binding mitochondrial carrier protein Aralar1 protein (202-317AA)
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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,SLC25A12 Antibody (CSB-PA021478LA01HU),的标记方式是Non-conjugated。对于SLC25A12 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, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 IHC 1:20-1:200 -
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:Mitochondrial and calcium-binding carrier that catalyzes the calcium-dependent exchange of cytoplasmic glutamate with mitochondrial aspartate across the mitochondrial inner membrane. May have a function in the urea cycle.
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基因功能参考文献:
- Genetic variants of SLC25A12 may be associated with risks for childhood ASD. PMID: 28536923
- The features of AGC1 structure and function in physiology and pathology, regulation by calcium, dependency on mitochondrial membrane potential, role in cancer cells, and tissue specificity are reviewed. AGC1 is involved in the glutamate-mediated excitotoxicity in neurons and AGC gene or protein alterations were discovered in rare human diseases. Review. PMID: 27132995
- Sensitivity analyses including only studies with family-based design demonstrated significant association between autism spectrum disorders and SNPs rs2292813 and rs2056202. In contrast, sensitivity analyses including case-control design studies only failed to find a significant association. Review. PMID: 25663199
- rs2056202 and rs2292813 in SLC25A12 may contribute significantly to autism spectrum disorders risk. PMID: 25921325
- Structure of the calcium bound and calcium free N- and C-terminal domains is described, elucidating the mechanism of calcium regulation. PMID: 25410934
- The physiological roles of AGC1, its links to calcium homeostasis, and its involvement in autism pathogenesis, are reviewed. PMID: 21691713
- This study found no differences in the allele, genotype, or haplotype frequencies of these two SNPs between patients and controls. PMID: 19913066
- Variants of the AGC1-encoding SLC25A12 gene were neither correlated with AGC activation nor associated with autism-spectrum disorders in 309 simplex and 17 multiplex families. PMID: 18607376
- SLC25A12 gene is linked to autism PMID: 15056512
- Aralar1 has a role in determining glucose metabolic fate, mitochondrial activity, and insulin secretion in beta cells PMID: 15494407
- These results suggest that SLC25A12 is not a major contributor to autism risk in these families. PMID: 16648338
- it is unlikely that the SLC25A12 polymorphisms investigated play a substantial role in conferring susceptibility to schizophrenia PMID: 17693006
- rs2056202 polymorphism in SLC25A12 may be associated with levels of routines and rituals in autism and related disorders PMID: 17894412
- SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects. PMID: 18180767
- SLC25A12 gene is associated with autism. PMID: 19360665
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相关疾病:Epileptic encephalopathy, early infantile, 39 (EIEE39)
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亚细胞定位:Mitochondrion inner membrane; Multi-pass membrane protein.
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蛋白家族:Mitochondrial carrier (TC 2.A.29) family
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组织特异性:Expressed predominantly in the heart and skeletal muscle, weakly in brain and kidney.
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数据库链接:
HGNC: 10982
OMIM: 603667
KEGG: hsa:8604
STRING: 9606.ENSP00000388658
UniGene: Hs.470608
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