EFR3A 抗体
-
- 抗原 See all EFR3A 抗体
- EFR3A (EFR3 Homolog A (EFR3A))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This EFR3A 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 EFR3A
- 亚型
- IgG
- Top Product
- Discover our top product EFR3A Primary Antibody
-
anti-EFR3 Homolog A (EFR3A) (AA 636-664), (C-Term) antibody
EFR3A 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB25694 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
- EFR3A (EFR3 Homolog A (EFR3A))
- 别名
- EFR3A (EFR3A 产品)
- 别名
- RGD1305976 antibody, A130089M23Rik antibody, BB071175 antibody, C76891 antibody, C920006C10Rik antibody, D030063F01Rik antibody, mKIAA0143 antibody, EFR3 homolog A antibody, EFR3 homolog A L homeolog antibody, Efr3a antibody, EFR3A antibody, efr3a.L antibody
- 背景
-
Synonyms: EFR 3A, EFR3 homolog A S. cerevisiae, EFR3 homolog A, KIAA0143, Protein EFR3 homolog A, Protein EFR3 like,
Background: EFR3A is a plasma membrane protein that contains 821 amino acids and belongs to the EFR3 family. EFR3A is alternatively spliced creating three isoforms and is encoded by a gene that maps to human chromosome 8. Human chromosome 8 consists of nearly 146 million base pairs, encodes over 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
- 基因ID
- 23167
-
