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    PAX6 / Cy5 (bs-22254R-Cy5)  
    訂購熱線:400-901-9800
    訂購郵箱:sales@bioss.com.cn
    訂購QQ:  400-901-9800
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    100ul/2980.00元
    大包裝/詢價
    產品編號 bs-22254R-Cy5
    英文名稱 PAX6 / Cy5
    中文名稱 Cy5標記的轉錄因子Pax6抗體
    別    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.  
    研究領域 發育生物學  神經生物學  干細胞  
    抗體來源 Rabbit
    克隆類型 Polyclonal
    交叉反應
    產品應用
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 46kDa
    細胞定位 細胞核 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human PAX6: 221-320/422 
    亞    型 IgG
    純化方法 affinity purified by Protein A
    緩 沖 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產品介紹 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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