Ferric-Chelate Reductase 1 Like (FRRS1L) 抗体
Quick Overview for Ferric-Chelate Reductase 1 Like (FRRS1L) 抗体 (ABIN1387966)
抗原
See all Ferric-Chelate Reductase 1 Like (FRRS1L) 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human Brain protein CG6
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亚型
- IgG
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anti-Ferric-Chelate Reductase 1 Like (FRRS1L) (AA 158-267) antibody
FRRS1L 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Ferric-Chelate Reductase 1 Like (FRRS1L) (AA 74-123) antibodyFRRS1L 适用: 人, Cow, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Ferric-Chelate Reductase 1 Like (FRRS1L) (AA 215-264) antibodyFRRS1L 适用: 人, Cow, Pig, 小鼠, 犬, 马, 兔, 猴, 小鸡, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Ferric-Chelate Reductase 1 Like (FRRS1L) (N-Term) antibodyFRRS1L 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Ferric-Chelate Reductase 1 Like (FRRS1L) (N-Term) antibodyFRRS1L 适用: 人, 大鼠, Cow, Pig, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Ferric-Chelate Reductase 1 Like (FRRS1L) (Middle Region) antibodyFRRS1L 适用: 人, 大鼠, Cow, Pig, 小鼠, 犬, 马, 兔, 豚鼠, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- Ferric-Chelate Reductase 1 Like (FRRS1L)
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别名
- Brain protein CG6
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背景
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Synonyms: Brain protein CG 6, Brain protein CG-6, Brain protein CG6, C9orf4, CG 6, CG6, chromosome 9 open reading frame 4, CI004_HUMAN, Uncharacterized protein C9orf4.
Background: C9orf4 is a 344 amino acid single-pass membrane protein that is primarily expressed in adult and fetal brain and is weakly expressed in spinal cord, adult ovary and medulla. C9orf4 contains one DOMON domain, a predominantly _-sheet domain that is thought to aide in extracellular adhesion. The gene encoding C9orf4 maps to human chromosome 9, which consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
抗原
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