CXX1 抗体
(1 reference)-
- 抗原 See all CXX1 (FAM127A) 抗体
- CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
- 适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This CXX1 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Flow Cytometry (FACS), 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 CXX1/Cerebral protein 5
- 亚型
- IgG
-
anti-Family with Sequence Similarity 127, Member A (FAM127A) (AA 1-209) antibody
FAM127A 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Family with Sequence Similarity 127, Member A (FAM127A) (AA 1-113) antibodyFAM127A 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
FCM 1:20-100
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
-
-
: "Selective expression of sense and antisense transcripts of the sushi-ichi-related retrotransposon--derived family during mouse placentogenesis." in: Retrovirology, Vol. 12, pp. 9, (2015) (PubMed).
-
: "Selective expression of sense and antisense transcripts of the sushi-ichi-related retrotransposon--derived family during mouse placentogenesis." in: Retrovirology, Vol. 12, pp. 9, (2015) (PubMed).
-
- 抗原
- CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
- 别名
- Cerebral protein 5 (FAM127A 产品)
- 别名
- CXX1 antibody, MAR8C antibody, MART8C antibody, Mar8 antibody, Mart8 antibody, retrotransposon Gag like 8C antibody, RTL8C antibody
- 背景
-
Synonyms: Mammalian retrotransposon derived protein 8C, CAAX box protein 1, Cerebral protein 5, CXX 1, FAM127A, Family with sequence similarity 127, member A, Mar8, MAR8C, Mart8, F127A_HUMAN.
Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXX1 gene product has been provisionally designated CXX1 pending further characterization.
- 基因ID
- 8933
-
