C12ORF24 抗体 (AA 195-245) (Biotin)
-
- 抗原 See all C12ORF24 (C12orf24) products
- C12ORF24 (C12orf24) (Chromosome 12 Open Reading Frame 24 (C12orf24))
-
抗原表位
- AA 195-245
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C12ORF24 antibody is conjugated to Biotin
-
应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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 C12ORF24
- 亚型
- IgG
-
anti-Chromosome 12 Open Reading Frame 24 (C12orf24) (AA 1-273) antibody
C12orf24 适用: 人 WB, ELISA, IP 宿主: 小鼠 Monoclonal 2G4-1A1 unconjugated
anti-Chromosome 12 Open Reading Frame 24 (C12orf24) (AA 1-273) antibodyC12orf24 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 24 (C12orf24) (AA 38-87) antibodyC12orf24 适用: 人, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 24 (C12orf24) (N-Term) antibodyC12orf24 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 12 Open Reading Frame 24 (C12orf24) (N-Term) antibodyC12orf24 适用: 人, Pig, Cow WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
IHC-P 1:200-400 - 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 for 12 months.
- 有效期
- 12 months
-
- 抗原
- C12ORF24 (C12orf24) (Chromosome 12 Open Reading Frame 24 (C12orf24))
- 别名
- C12ORF24 (C12orf24 产品)
- 别名
- C12orf24 antibody, C17H12orf24 antibody, HSU79274 antibody, 1500011H22Rik antibody, family with sequence similarity 216 member A antibody, family with sequence similarity 216, member A antibody, FAM216A antibody, Fam216a antibody
- 背景
-
Synonyms: Chromosome 12 open reading frame 24, HSU79274, Hypothetical protein LOC29902, Protein predicted by clone 23733, F216A_HUMAN, Protein FAM216A, FAM216A.
Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf24 gene product has been provisionally designated C12orf24 pending further characterization.
- 基因ID
- 29902
- UniProt
- Q8WUB2
-
