蛋白
抗体
检测试剂盒
蛋白MARKER
分子生物学
规格：
查看说明书FACL4 Rabbit pAb
Cat#:DPA01726应用：WB,IHC,ICC/IF
| Product Name: | FACL4 Rabbit pAb |
| Cat No.: | DPA02256 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human |
| Tested Applications: | WB,IHC,ICC/IF,FC,IP |
| Recommended Dilution: | WB: 1:1000 IHC: 1:100 ICC/IF: 1:20 FC: 1:20 IP: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | Recombinant protein of human FACL4 |
| Calculated Molecular Weight: | 79 kDa |
| Observed Molecular Weight: | 79 kDa |
| GenBank Accession Number: | O60488 |
| Gene ID (NCBI): | 2182 |
| Synonyms: | ACS4; FACL4; LACS4; MRX63; MRX68 |
| Background: | The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016] |
| Category: | Primary Ab |
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