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- 靶点-Target: ALS2
- MW(Observed): 182kD
- 宿主物种-Host Species: Rabbit
- 同种型-Isotype: IgG
- 修饰-Modification: Unmodified
- 推荐稀释比: WB 1:500-2000;ELISA 1:5000-20000
- 组成: PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
- 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
- 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
- 浓度: 1 mg/ml
- 克隆性: Polyclonal
- 免疫原: Synthesized peptide derived from human protein . at AA range: 390-470
- 特异性: ALS2 Polyclonal Antibody detects endogenous levels of protein.
- 基因名称: ALS2 ALS2CR6 KIAA1563
- 蛋白名称: Alsin (Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 6 protein) (Amyotrophic lateral sclerosis 2 protein)
- Organism-1: Human
- 基因ID-1: 57679
- SwissProt-1: Q96Q42
- Organism-2: Mouse
- SwissProt-2: Q920R0
- Organism-3: Rat
- SwissProt-3: P0C5Y8
- 背景: The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008],
- 细胞定位: ruffle,early endosome,centrosome,cytosol,postsynaptic density,membrane,lamellipodium,axon,dendrite,growth cone,vesicle,neuronal cell body,dendritic spine,intracellular membra