PTCHD4 抗体 (AA 1-100) (HRP)
Quick Overview for PTCHD4 抗体 (AA 1-100) (HRP) (ABIN1712207)
抗原
适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 1-100
-
预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit
-
纯化方法
- Purified by Protein A.
-
免疫原
- KLH conjugated synthetic peptide derived from human C6orf138
-
亚型
- IgG
-
-
anti-Patched Domain Containing 4 (PTCHD4) (AA 563-591) antibody
PTCHD4 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB29403 unconjugated
anti-Patched Domain Containing 4 (PTCHD4) (AA 570-599), (Middle Region) antibodyPTCHD4 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
-
WB 1:300-5000
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
-
-
- PTCHD4 (Patched Domain Containing 4 (PTCHD4))
-
别名
- C6orf138
-
背景
-
Synonyms: C6orf138, PTHD4_HUMAN, Patched domain-containing protein C6orf138.
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 C6orf138 gene product has been provisionally designated C6orf138 pending further characterization.
-
基因ID
- 442213
抗原
-
