EMID1 抗体 (AA 351-441) (Alexa Fluor 555)
-
- 抗原 See all EMID1 products
- EMID1 (EMI Domain Containing 1 (EMID1))
-
抗原表位
- AA 351-441
-
适用
- 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This EMID1 antibody is conjugated to Alexa Fluor 555
-
应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse,Dog,Cow
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human EMID1
- 亚型
- IgG
-
anti-EMI Domain Containing 1 (EMID1) antibody
EMID1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-EMI Domain Containing 1 (EMID1) (C-Term) antibodyEMID1 适用: 人, 大鼠, 小鼠, Cow, 犬, 马 WB 宿主: 兔 Polyclonal unconjugated
anti-EMI Domain Containing 1 (EMID1) (C-Term) antibodyEMID1 适用: 人, 大鼠, 小鼠, Cow, 犬, 马, 豚鼠 WB 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
-
- 抗原
- EMID1 (EMI Domain Containing 1 (EMID1))
- 别名
- EMID1 (EMID1 产品)
- 别名
- EMI5 antibody, EMU1 antibody, AW122071 antibody, CO-5 antibody, Emu1 antibody, RGD1565846 antibody, EMI domain containing 1 antibody, EMID1 antibody, Emid1 antibody
- 背景
-
Synonyms: AW122071, CO 5, CTA-984G1.2, EMI domain containing 1, EMI domain containing protein 1, EMI domain-containing protein 1, EMI5, EMID 1, Emid1, EMID1_HUMAN, Emilin and multimerin domain containing protein 1, Emilin and multimerin domain-containing protein 1, EMU1, hEmu1, MGC50657, OTTMUSP00000005297, Protein Emu1, Putative emu1, RGD1565846, RP23-338J18.3.
Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
- 基因ID
- 129080
- UniProt
- Q96A84
-
