HIAT1 抗体 (PE-Cy5.5)
Quick Overview for HIAT1 抗体 (PE-Cy5.5) (ABIN900694)
抗原
适用
宿主
克隆类型
标记
应用范围
-
-
交叉反应
- 小鼠
-
预测反应
- Human,Rat,Cow,Horse
-
纯化方法
- Purified by Protein A.
-
免疫原
- KLH conjugated synthetic peptide derived from human HIAT1
-
亚型
- IgG
-
-
anti-Hippocampus Abundant Transcript 1 (HIAT1) (AA 454-483), (C-Term) antibody
HIAT1 适用: 小鼠, 人, Hamster WB, IHC (p) 宿主: 兔 Polyclonal RB25772 unconjugated
anti-Hippocampus Abundant Transcript 1 (HIAT1) (AA 460-490), (C-Term) antibodyHIAT1 适用: 小鼠, 人, Hamster WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
-
-
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
- Sodium azide
-
注意事项
- This product contains sodium azide: 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
-
-
- HIAT1 (Hippocampus Abundant Transcript 1 (HIAT1))
-
别名
- HIAT1
-
背景
-
Synonyms: Hippocampus abundant gene transcript 1, Hippocampus abundant transcript, Hippocampus abundant transcript 1, Putative tetracycline transporter like protein, Tetracycline transporter like prot, MGC144858, rCG_28876, DKFZp564L0864, HIAT1_HUMAN.
Background: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
-
分子量
- 53kDa
-
基因ID
- 64645
抗原
-
