C11orf57 抗体
-
- 抗原 See all C11orf57 products
- C11orf57 (Chromosome 11 Open Reading Frame 57 (C11orf57))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C11orf57 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), 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 C11orf57
- 亚型
- IgG
-
anti-Chromosome 11 Open Reading Frame 57 (C11orf57) (AA 179-228) antibody
C11orf57 适用: 人, Cow, 犬, 豚鼠, 兔, Pig, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 11 Open Reading Frame 57 (C11orf57) (AA 107-156) antibodyC11orf57 适用: 人, 小鼠, Cow, 犬, 豚鼠, Pig WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
-
- 抗原
- C11orf57 (Chromosome 11 Open Reading Frame 57 (C11orf57))
- 别名
- C11orf57 (C11orf57 产品)
- 别名
- NKAP domain containing 1 antibody, chromosome 24 C11orf57 homolog antibody, NKAP domain containing 1 L homeolog antibody, NKAPD1 antibody, C24H11orf57 antibody, nkapd1 antibody, nkapd1.L antibody
- 背景
-
Synonyms: chromosome 11 open reading frame 57, CK057_HUMAN, FLJ10726, hypothetical protein LOC55216, Uncharacterized protein C11orf57.
Background: C11orf57, also known as FLJ10726, is a 292 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
- 基因ID
- 55216
-
