CCDC170 抗体 (AA 451-550) (Cy3)
Quick Overview for CCDC170 抗体 (AA 451-550) (Cy3) (ABIN1703292)
抗原
See all CCDC170 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 451-550
-
预测反应
- Human,Mouse,Rat,Cow,Pig,Horse
-
纯化方法
- Purified by Protein A.
-
免疫原
- KLH conjugated synthetic peptide derived from human C6orf97
-
亚型
- IgG
-
-
anti-Coiled-Coil Domain Containing 170 (CCDC170) (C-Term) antibody
CCDC170 适用: 人 WB, IHC (p), ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 170 (CCDC170) (AA 442-715) antibodyCCDC170 适用: 人 WB, IHC (p), ICC, IHC 宿主: 兔 Polyclonal unconjugated
-
-
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
-
-
- CCDC170 (Coiled-Coil Domain Containing 170 (CCDC170))
-
别名
- C6orf97
-
背景
-
Synonyms: bA282P11.1, C6orf97, CC170_HUMAN, Chromosome 6 open reading frame 97, Coiled coil domain containing protein C6orf97, Coiled-coil domain-containing protein C6orf97, FLJ23305, Hypothetical protein LOC80129, LOC80129.
Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf97 gene product has been provisionally designated C6orf97 pending further characterization.
-
基因ID
- 80129
抗原
-
