锚蛋白重复结构域蛋白22抗体

产品货号：

BN41404R
中文名称：

锚蛋白重复结构域蛋白22抗体
英文名称：

Rabbit anti-ANKRD22 Polyclonal antibody
品牌：

Biorigin

货号

产品规格

售价

备注
BN41404R-100ul

100ul

¥2120.00

交叉反应（总）:Human,Mouse,Rat,Dog,Pig,Cow,Horse,Rabbit,Sheep,;推荐应用:WB,
BN41404R-200ul

200ul

¥3140.00

交叉反应（总）:Human,Mouse,Rat,Dog,Pig,Cow,Horse,Rabbit,Sheep,;推荐应用:WB,

产品描述

英文名称	ANKRD22
中文名称	锚蛋白重复结构域蛋白22抗体
别名	Ankrd22; Ankyrin repeat domain 22; Ankyrin repeat domain-containing protein 22; ANR22_HUMAN.
研究领域	细胞生物免疫学
抗体来源	Rabbit
克隆类型	Polyclonal
交叉反应	Human, Mouse, (predicted: Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
产品应用	WB=1:500-2000 ELISA=1:5000-10000 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分子量	22kDa
细胞定位	细胞核细胞浆细胞膜细胞外基质分泌型蛋白
性状	Liquid
浓度	1mg/ml
免疫原	KLH conjugated synthetic peptide derived from human ANKRD22:51-150/191
亚型	IgG
纯化方法	affinity purified by Protein A
储存液	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMed	PubMed
产品介绍	Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria. Similarity: Contains 4 ANK repeats. SWISS: Q5VYY1 Gene ID: 118932 Database links: Entrez Gene: 118932 Human Entrez Gene: 52024 Mouse SwissProt: Q5VYY1 Human SwissProt: Q9D3J5 Mouse Unigene: 217484 Human Unigene: 183030 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.