C2ORF16 抗体 (AA 1901-1984) (HRP)
-
- 抗原 See all C2ORF16 products
- C2ORF16 (Chromosome 2 Open Reading Frame 16 (C2ORF16))
- 抗原表位
- AA 1901-1984
- 适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C2ORF16 antibody is conjugated to HRP
-
应用范围
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C2orf16
- 亚型
- IgG
-
anti-Chromosome 2 Open Reading Frame 16 (C2ORF16) (AA 1901-1984) antibody
C2ORF16 适用: 人 IF (cc), IF (p), IHC (p), ELISA, IHC (fro), ICC 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
IHC-P 1:200-400
IHC-F 1:100-500 - 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.
- 注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- 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
- C2ORF16 (Chromosome 2 Open Reading Frame 16 (C2ORF16))
- 别名
- C2orf16 (C2ORF16 产品)
- 别名
- chromosome 2 open reading frame 16 antibody, C2orf16 antibody
- 背景
-
Synonyms: Uncharacterized protein C2orf16, C2orf16
Background: C2orf16 (chromosome 2 open reading frame 16), also known as DKFZp434G118 or DKFZp781D2023, is a 1,984 amino acid protein encoded by a gene that maps to human chromosome 2p23.3. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
- 基因ID
- 84226
- UniProt
- Q68DN1
-
