Kyphoscoliosis Peptidase 抗体 (AA 51-150) (Alexa Fluor 488)
-
- 抗原 See all Kyphoscoliosis Peptidase (KY) 抗体
- Kyphoscoliosis Peptidase (KY)
-
抗原表位
- AA 51-150
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This Kyphoscoliosis Peptidase antibody is conjugated to Alexa Fluor 488
-
应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Kyphoscoliosis peptidase
- 亚型
- IgG
- Top Product
- Discover our top product KY Primary Antibody
-
anti-Kyphoscoliosis Peptidase (KY) antibody (PE)
KY 适用: Pig FACS 宿主: 小鼠 Monoclonal 76-7-4 PE
anti-Kyphoscoliosis Peptidase (KY) antibodyKY 适用: Pig FACS 宿主: 小鼠 Monoclonal 76-7-4 unconjugated
anti-Kyphoscoliosis Peptidase (KY) antibody (Biotin)KY 适用: Pig FACS 宿主: 小鼠 Monoclonal 76-7-4 Biotin
anti-Kyphoscoliosis Peptidase (KY) antibody (FITC)KY 适用: Pig FACS 宿主: 小鼠 Monoclonal 76-7-4 FITC
-
- 应用备注
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
-
- 抗原
- Kyphoscoliosis Peptidase (KY)
- 别名
- KY/Kyphoscoliosis peptidase (KY 产品)
- 别名
- CD1 antibody, D9Mgc44e antibody, ky antibody, kyphoscoliosis peptidase antibody, Ky antibody, KY antibody
- 背景
-
Synonyms: KY, KY_HUMAN, Kyphoscoliosis peptidase.
Background: KY peptidase (Kyphoscoliosis peptidase) is a 561 amino acid cytoskeleton protease that interacts with several sarcomeric cytoskeletal proteins, including Filamin 2. KY peptidase probably plays a role in the maturation, function and stabilization of the neuromuscular junction. KY-null mouse mutants exhibit distinct irregular subceullular Filamin 2 localization, suggesting that KY peptidase deficiency may be the cause of several types of limb-girdle muscular dystrophies.
- 基因ID
- 339855
- 途径
- Skeletal Muscle Fiber Development
-
