Anti-ISCU Antibody (CAB7082)
- SKU:
- CAB7082
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
| 抗体名: | Anti-ISCU Antibody |
| 抗体コード: | CAB7082 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | WB |
| 反応性: | Human |
| 宿主種: | Rabbit |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-167 of human ISCU (NP_998760.1). |
| 申し込み: | WB |
| 推奨希釈: | WB 1:500 - 1:2000 |
| 反応性: | Human |
| ポジティブサンプル: | HT-1080, U-87MG, 293T, A-549, HeLa |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-167 of human ISCU (NP_998760.1). |
| 精製方法: | Affinity purification |
| ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| アイソタイプ: | IgG |
| 順序: | MAAA GAFR LRRA ASAL LLRS PRLP AREL SAPA RLYH KKVV DHYE NPRN VGSL DKTS KNVG TGLV GAPA CGDV MKLQ IQVD EKGK IVDA RFKT FGCG SAIA SSSL ATEW VKGK TVEE ALTI KNTD IAKE LCLP PVKL HCSM LAED AIKA ALAD YKLK QEPK KGEA EKK |
| 遺伝子ID: | 23479 |
| Uniprot: | Q9H1K1 |
| セルラーロケーション: | Cytoplasm, Mitochondrion, Nucleus |
| 計算された分子量: | 15kDa/17kDa |
| 観察された分子量: | 14-18kDa |
| 同義語: | ISCU, 2310020H20Rik, HML, ISU2, NIFU, NIFUN, hnifU |
| バックグラウンド: | This gene encodes a component of the iron-sulfur (Fe-S) cluster scaffold. Fe-S clusters are cofactors that play a role in the function of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, and oxidative stress response. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol or to the mitochondrion. Mutations in this gene have been found in patients with hereditary myopathy with lactic acidosis. A disease-associated mutation in an intron may activate a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein. A pseudogene of this gene is present on chromosome 1. |
| UniProt Protein Function: | ISCU: Involved in the assembly or repair of the [Fe-S] clusters present in iron-sulfur proteins. Binds iron. Defects in ISCU are the cause of myopathy with exercise intolerance Swedish type (MEIS); also known as myopathy with deficiency of succinate dehydrogenase and aconitase or myoglobinuria due to abnormal glycolysis or hereditary myopathy with lactic acidosis (HML). This autosomal recessive metabolic disease is characterized by lifelong severe exercise intolerance, in which minor exertion causes fatigue of active muscles, shortness of breath, and cardiac palpitations in association with lactic acidosis. The biochemical phenotype is characterized by a deficiency in mitochondrial iron-sulfur proteins and impaired muscle oxidative metabolism. Belongs to the NifU family. 2 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Mitochondrial Chromosomal Location of Human Ortholog: 12q24.1 Cellular Component: mitochondrion; mitochondrial matrix; cytoplasm; cytosol; nucleus Molecular Function:protein binding; iron ion binding; iron-sulfur cluster binding; protein complex scaffold Biological Process: iron-sulfur cluster assembly; nitrogen fixation Disease: Myopathy With Lactic Acidosis, Hereditary |
| NCBI Summary: | This gene encodes a component of the iron-sulfur (Fe-S) cluster scaffold. Fe-S clusters are cofactors that play a role in the function of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, and oxidative stress response. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol or to the mitochondrion. Mutations in this gene have been found in patients with hereditary myopathy with lactic acidosis. A disease-associated mutation in an intron may activate a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein. A pseudogene of this gene is present on chromosome 1. [provided by RefSeq, Feb 2016] |
| UniProt Code: | Q9H1K1 |
| NCBI GenInfo Identifier: | 313104118 |
| NCBI Gene ID: | 23479 |
| NCBI Accession: | Q9H1K1.2 |
| UniProt Related Accession: | Q9H1K1 |
| Molecular Weight: | 18kDa |
| NCBI Full Name: | Iron-sulfur cluster assembly enzyme ISCU, mitochondrial |
| NCBI Synonym Full Names: | iron-sulfur cluster assembly enzyme |
| NCBI Official Symbol: | ISCU |
| NCBI Official Synonym Symbols: | HML; ISU2; NIFU; NIFUN; hnifU; 2310020H20Rik |
| NCBI Protein Information: | iron-sulfur cluster assembly enzyme ISCU, mitochondrial |
| UniProt Protein Name: | Iron-sulfur cluster assembly enzyme ISCU, mitochondrial |
| UniProt Synonym Protein Names: | NifU-like N-terminal domain-containing protein; NifU-like protein |
| Protein Family: | Iron-sulfur cluster assembly enzyme |
| UniProt Gene Name: | ISCU |
| UniProt Entry Name: | ISCU_HUMAN |
 | Western blot analysis of extracts of various cell lines, using ISCU Antibody (CAB7082) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit (RM00021). Exposure time: 10s. |
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