Anti-FTL Antibody (CAB18051)[KO Validated]
![Anti-FTL Antibody (CAB18051)[KO Validated]](https://cdn11.bigcommerce.com/s-d5atsu6k01/images/stencil/608x608/products/17977/17844/anti-ftl-antibody-cab18051ko-validated__82590__79284.1645803851.jpg?c=1 "Anti-FTL Antibody (CAB18051)[KO Validated]")
- SKU:
- CAB18051
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
![Anti-FTL Antibody (CAB18051)[KO Validated]](https://cdn11.bigcommerce.com/s-d5atsu6k01/images/stencil/1280x1280/products/17977/17844/anti-ftl-antibody-cab18051ko-validated__82590__79284.1645803851.jpg?c=1&imbypass=on "Anti-FTL Antibody (CAB18051)[KO Validated]")
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Description
| 抗体名: | Anti-FTL Antibody [KO Validated] |
| 抗体コード: | CAB18051 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | WB IHC IF |
| 反応性: | Human, Mouse |
| 宿主種: | Rabbit |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-175 of human FTL (NP_000137.2). |
| 申し込み: | WB IHC IF |
| 推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:10 - 1:100 |
| 反応性: | Human, Mouse |
| ポジティブサンプル: | 293T |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-175 of human FTL (NP_000137.2). |
| 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: | MSSQ IRQN YSTD VEAA VNSL VNLY LQAS YTYL SLGF YFDR DDVA LEGV SHFF RELA EEKR EGYE RLLK MQNQ RGGR ALFQ DIKK PAED EWGK TPDA MKAA MALE KKLN QALL DLHA LGSA RTDP HLCD FLET HFLD EEVK LIKK MGDH LTNL HRLG GPEA GLGE YLFE RLTL KHD |
| 遺伝子ID: | 2512 |
| Uniprot: | P02792 |
| セルラーロケーション: | |
| 計算された分子量: | 20kDa |
| 観察された分子量: | 18kDa |
![Anti-FTL Antibody [KO Validated] (CAB18051)](https://cdn11.bigcommerce.com/s-h68l9z2lnx/product_images/d/876/A18051_1__27951.jpg) | Western blot analysis of extracts from normal (control) and FTL knockout (KO) 293T cells, using FTL antibody (CAB18051) at 1:500 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 Basic Kit (RM00020). Exposure time: 60s. |
| 同義語: | FTL, LFTD, NBIA3 |
| バックグラウンド: | This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes. |
| UniProt Protein Function: | FTL: Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. Also plays a role in delivery of iron to cells. Mediates iron uptake in capsule cells of the developing kidney. Defects in FTL are the cause of hereditary hyperferritinemia-cataract syndrome (HHCS). It is an autosomal dominant disease characterized by early-onset bilateral cataract. Affected patients have elevated level of circulating ferritin. HHCS is caused by mutations in the iron responsive element (IRE) of the FTL gene. Defects in FTL are the cause of neurodegeneration with brain iron accumulation type 3 (NBIA3); also known as adult-onset basal ganglia disease. It is a movement disorder with heterogeneous presentations starting in the fourth to sixth decade. It is characterized by a variety of neurological signs including parkinsonism, ataxia, corticospinal signs, mild nonprogressive cognitive deficit and episodic psychosis. It is linked with decreased serum ferritin levels. Belongs to the ferritin family. |
| UniProt Protein Details: | Protein type:Oxidoreductase Chromosomal Location of Human Ortholog: 19q13.33 Cellular Component: ferritin complex; membrane; cytosol Molecular Function:identical protein binding; protein binding; ferric iron binding; iron ion binding Biological Process: receptor-mediated endocytosis; iron ion homeostasis; cellular iron ion homeostasis; post-Golgi vesicle-mediated transport; iron ion transport; transmembrane transport Disease: Hyperferritinemia With Or Without Cataract; L-ferritin Deficiency; Neurodegeneration With Brain Iron Accumulation 3 |
| NCBI Summary: | This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes. [provided by RefSeq, Jul 2008] |
| UniProt Code: | P02792 |
| NCBI GenInfo Identifier: | 120523 |
| NCBI Gene ID: | 2512 |
| NCBI Accession: | P02792.2 |
| UniProt Secondary Accession: | P02792,Q6IBT7, Q7Z2W1, Q86WI9, Q8WU07, Q96AU9, Q96CU0 Q9BTZ8, B2R4B9, |
| UniProt Related Accession: | P02792 |
| Molecular Weight: | 440 kDa |
| NCBI Full Name: | Ferritin light chain |
| NCBI Synonym Full Names: | ferritin, light polypeptide |
| NCBI Official Symbol: | FTL |
| NCBI Official Synonym Symbols: | LFTD; NBIA3 |
| NCBI Protein Information: | ferritin light chain; ferritin L-chain; ferritin L subunit; ferritin light polypeptide-like 3 |
| UniProt Protein Name: | Ferritin light chain |
| Protein Family: | Ferritin |
| UniProt Gene Name: | FTL |
| UniProt Entry Name: | FRIL_HUMAN |