KIF1BP 抗体 (AA 180-220) (Cy3)
-
- 抗原 See all KIF1BP (KIAA1279) 抗体
- KIF1BP (KIAA1279) (KIAA1279)
-
抗原表位
- AA 180-220
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This KIF1BP antibody is conjugated to Cy3
-
应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human KBP
- 亚型
- IgG
- Top Product
- Discover our top product KIAA1279 Primary Antibody
-
-
- 应用备注
- IF(IHC-P) 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
- KIF1BP (KIAA1279) (KIAA1279)
- 别名
- KBP (KIAA1279 产品)
- 别名
- KBP antibody, TTC20 antibody, 0710007C18Rik antibody, mKIAA1279 antibody, Kbp antibody, CPi-21 antibody, GHR-P63 antibody, Klkbp antibody, SPI-2 antibody, SPI-2.3 antibody, SPI2 antibody, Serpina3k antibody, Spin2 antibody, Spin2b antibody, Kiaa1279 antibody, KIAA1279 antibody, kbp antibody, KIF1 binding protein antibody, serine (or cysteine) proteinase inhibitor, clade A, member 3C antibody, KIF1BP antibody, Kif1bp antibody, Serpina3c antibody
- 背景
-
Synonyms: Hypothetical protein LOC26128, KBP, KBP_HUMAN, KIAA1279, K1-binding protein, TTC20, Uncharacterized protein KIAA1279.
Background: Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.
- 基因ID
- 26128
- UniProt
- Q96EK5
-