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Rabbit Anti-PAX6, Alexa Fluor 488 conjugated antibody (bs-22254R-AF488)
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说明书: 100ul  
100ul/2980.00元
大包装/询价
产品编号 bs-22254R-AF488
英文名称 PAX6, Alexa Fluor 488 conjugated
中文名称 AF488标记的转录因子Pax6抗体
别    名 AN 2; AN antibody; AN2; Aniridia type II protein; D11S812E; MGC17209; MGDA; Oculorhombin; Paired box 6; Paired box gene 6 (aniridia keratitis); Paired Box Gene 6; Paired box homeotic gene 6; Paired box protein Pax-6; Paired box protein Pax6; PAX 6; PAX6; PAX6_HUMAN; Sey; WAGR.  
研究领域 发育生物学  神经生物学  干细胞  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应
产品应用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 46kDa
细胞定位 细胞核 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PAX6: 221-320/422 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 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.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 Pax genes contain paired domains with strong homology to genes in Drosophila which are involved in programming early development. The PAX2 gene is expressed in primitive cells of the kidney, ureter, eye, ear, and central nervous system. More specifically, in human embryo sections, PAX2 is expressed in the optic vesicle and later in the retina, in the otic vesicle and later in the semicircular canals of the inner ear, and in mesonephros, metanephros, adrenals, spinal cord, and hindbrain. PAX2 mutations can be responsible for renal hypoplasia, either isolated or associated with various ophthalmologic manifestations ranging from retinal coloboma to microphthalmia. The gene which encodes Pax-2 maps to human chromosome 10q24.3-q25.1. Lesions in the PAX6 gene accounts for most cases of aniridia, a congenital malformation of the eye, chiefly characterized by iris hypoplasia, which can cause blindness. PAX6 is involved in other anterior segment malformations besides aniridia, such as Peters anomaly, a major error in the embryonic development of the eye with corneal clouding with variable iridolenticulocorneal adhesions. The gene which encodes Pax-6 maps to human chromosome 11p13.

SWISS:
P26367

Gene ID:
5080

Database links:

Entrez Gene: 395943 Chicken

Entrez Gene: 286857 Cow

Entrez Gene: 5080 Human

Entrez Gene: 18508 Mouse

Entrez Gene: 25509 Rat

Entrez Gene: 30567 Zebrafish

Omim: 607108 Human

SwissProt: P47237 Chicken

SwissProt: Q1LZF1 Cow

SwissProt: P26367 Human

SwissProt: P63015 Mouse

SwissProt: P63016 Rat

SwissProt: P55864 Xenopus laevis

SwissProt: P26630 Zebrafish

Unigene: 270303 Human

Unigene: 611376 Human

Unigene: 33870 Mouse

Unigene: 3608 Mouse

Unigene: 89724 Rat

Unigene: 647 Xenopus laevis

Unigene: 24244 Zebrafish



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