HIGD1A 抗体 (HRP)
Quick Overview for HIGD1A 抗体 (HRP) (ABIN1418512)
抗原
See all HIGD1A 抗体适用
宿主
克隆类型
标记
应用范围
-
-
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 HIG1/HIGD1A
-
亚型
- IgG
-
-
anti-HIG1 Hypoxia Inducible Domain Family, Member 1A (HIGD1A) (AA 1-93) antibody
HIGD1A 适用: 人 WB, IF, IHC 宿主: 兔 Polyclonal unconjugated
anti-HIG1 Hypoxia Inducible Domain Family, Member 1A (HIGD1A) (N-Term) antibodyHIGD1A 适用: 人 WB, IF, EIA 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- IHC-P 1:200-400
-
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.
-
注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
-
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
-
-
- HIGD1A (HIG1 Hypoxia Inducible Domain Family, Member 1A (HIGD1A))
-
别名
- HIG1
-
背景
-
Synonyms: Hig1, HIG1 domain family member 1A, HIG1 domain family, member 1A, HIG1 hypoxia inducible domain family, member 1A, HIG1A_HUMAN, HIGD1A, HIMP1, Hypoxia-inducible gene 1 protein.
Background: HIGD1A (HIG1 domain family member 1A), also known as HIG1 (hypoxia-inducible gene 1 protein) or HSPC010, is a 93 amino acid multi-pass membrane protein that contains one HIG1 domain. Existing as two alternatively spliced isoforms, the gene encoding HIGD1A maps to human chromosome 3, which contains approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
-
基因ID
- 25994
抗原
-
