Prosci/ACADM Antibody/25-092/50 ug
商品编号：
25-092
品牌：
prosci-inc
市场价：
¥6500.00
美元价：
3900.00
产品分类：
重组抗体
公司分类：
Recombinant_antibodies
联系Q Q：
3392242852
电话号码：
4000-520-616
电子邮箱：
info@ebiomall.com
商品介绍
Specifications
| SPECIES REACTIVITY: | Human |
|---|---|
| TESTED APPLICATIONS: | ELISA, WB |
| APPLICATIONS: | ACADM antibody can be used for detection of ACADM by ELISA at 1:1562500. ACADM antibody can be used for detection of ACADM by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000. |
| USER NOTE: | Optimal dilutions for each application to be determined by the researcher. |
| POSITIVE CONTROL: | 1) 721_B Cell Lysate |
| PREDICTED MOLECULAR WEIGHT: | 46 kDa |
| IMMUNOGEN: | Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ACADM. |
| HOST SPECIES: | Rabbit |
Properties
| PURIFICATION: | Antibody is purified by peptide affinity chromatography method. |
|---|---|
| PHYSICAL STATE: | Lyophilized |
| BUFFER: | Antibody is lyophilized in PBS buffer with 2% sucrose. Add 50 μL of distilled water. Final antibody concentration is 1 mg/mL. |
| CONCENTRATION: | 1 mg/ml |
| STORAGE CONDITIONS: | For short periods of storage (days) store at 4˚C. For longer periods of storage, store ACADM antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles. |
| CLONALITY: | Polyclonal |
| CONJUGATE: | Unconjugated |
Additional Info
| ALTERNATE NAMES: | ACADM, ACAD1, MCAD, MCADH |
|---|---|
| ACCESSION NO.: | NP_000007 |
| PROTEIN GI NO.: | 4557231 |
| OFFICIAL SYMBOL: | ACADM |
| GENE ID: | 34 |
Background
| BACKGROUND: | ACADM Is the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Clinical phenotypes are associated with ACADM hereditary deficiency.This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
|---|---|
| REFERENCES: | 1) Nichols, M.J., (2008) Am. J. Med. Genet. A 146A (5), 610-619. |
品牌介绍
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