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葡糖酸内酯号：90-80-2
英文名称：D-(+)-Gluconic acid δ-lactone；D-Gluco,5-lactone；D(+)-Gluconolactone；Gluconodeltalactone；α,β,γ-Trihydroxy-δ-hydroxy-methyl-δ-alerolactone；β,γ,ε-Tetrahydroxy-δ-caprolactone；Fujiglucon
其他名称：葡萄糖内酯；葡萄糖酸内酯；葡糖醛酸内酯；葡醛酯；葡醛酸；D-葡萄糖酸-δ-内酯；1,5-葡萄糖酸内酯；克劳酸
号：90-80-2
C6H10O6=178.14
级别：BR
含量：≥99.0%
比旋光度：+60～+67°（C=10，H2O)
熔点：151～158℃
水溶液实验：澄清透明
重金属：≤0.002%
性状(以下信息仅供参考)：白色结晶粉末，无臭或略带气味。易溶于水，并缓慢水解，在水中溶解度为59g/100ml，稍溶于乙醇，在乙醇中为1g/100ml，不溶于乙迷。新配制的1%溶液pH为2.5。在水溶液中水解形成葡萄糖酸与其内酯的平衡溶液。密度:0.6
用途：本品仅供科研，不得用于其它用途
保存：RT，保质期2年客户根据葡糖酸内酯号：90-80-2 性质、化学式、分子式、结构式、比重、密度、号、沸点、熔点、水溶性、MSDS、用途、作用、规格包装、性状、注意事项、英文名、别称、纯度、级别等情况，本产品化学性质稳定，运输条件不苛刻，一般储存在阴凉，干燥，通风良好的地方，远离不相容的物质。保持容器密闭。
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包装：1kg、100g、10g、250g、25g、500g、50g、5g等包装
级别：GR级别、AR级别、CP级别、L.P.级别等
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Function : Probable transcription factor.
Subcellular Location : Nucleus.
Tissue Specificity : Expressed in testis.
DISEASE : Defects in SALL4 are the cause of Duane-radial ray syndrome (DRRS) [MIM:607323]; also known as Okihiro syndrome. DRRS is a disorder characterized by the association of forearm malformations with Duane retraction syndrome.
Defects in SALL4 are the cause of oculootoradial syndrome (OORS) [MIM:147750]. Oculootoradial s葡糖酸内酯号：90-80-2 yndrome is an autosomal dominant condition characterized by upper limbs anomalies (radial ray defects, carpal bones fusion), extraocular motor disturbances, congenital bilateral non-progressive mixed hearing loss. Other less consistent malformations include heart involvement, mild thrombocytopenia and leukocytosis (before age 50), shoulder girdle hypoplasia, imperforate anus, kidney malrotation or rectovaginal fistula. The IVIC syndrome is an allelic disorder of Duane-radial ray syndrome (DRRS) with a similar phenotype.
Similarity : Belongs to the sal C2H2-type zinc-finger protein family.
Contains 7 C2H2-type zinc fingers.
Database links : UniProtKB/Swiss-Prot: Q9UJQ4.1
英文名称 Anti-SOX17
中文名称 转录因子SOX17抗体
别 名 SOX-17; SOX17_HUMAN; SRY (sex determining region Y) box 17; SRY box 17; SRY related HMG box transcription factor SOX17; Transcription factor SOX-17; Transcription factor SOX17.
浓 度 1mg/1ml
规 格 0.2ml/200μg
抗体来源 Rabbit
克隆类型 polyclonal
交叉反应 Human, Mouse, Rat, Chicken, Pig, Cow
产品类型 一抗
研究领域 发育生物学 干细胞 转录调节因子 表观遗传学
蛋白分子量 predicted molecular weight: 44kDa
性 状 Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from Human SOX17
亚 型 IgG
纯化方法 affinity purified by Protein A
储 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500
（石蜡切片需做抗原修复）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍 Sox genes comprise a family of genes that are related to the mammalian sex determining gene SRY. These genes similarly contain sequences that encode for the HMG-box domain, which is responsible for the sequence-specific DNA-binding activity. Sox genes encode putative transcriptional regulators implicated in the decision of cell fates during development and the control of diverse developmental processes. The highly complex group of Sox genes cluster at least 40 different loci that rapidly diverged in various animal lineages. At present, 30 Sox genes have been identified. Members of this family have been shown to be conserved during evolution and to play key roles during animal development. Some are involved in human diseases, including sex reversal.
Function : Acts as transcription regulator that binds target promoter DNA and bends the DNA. Binds to the sequences 5'-AACAAT-'3 or 5'-AACAAAG-3'. Modulates transcriptional regulation via WNT3A. Inhibits Wnt signaling. Promotes degradation of activated CTNNB1. Plays a key role in the regulation of embryonic development. Required for normal looping of the embryonic heart tube. Required for normal development of the definitive gut endoderm. Probable transcriptional activator in the premeiotic germ cells.
Subunit : Interacts with CTNNB1, LEF1 and TCF4 (By similarity).
Subcellular Location : Nucleus.
Tissue Specificity : Expressed in adult heart, lung, spleen, testis, ovary, placenta, fetal lung, and kidney. In normal gastrointestinal tract, it is preferentially expressed in esophagus, stomach and small intestine than in colon and rectum.
DISEASE : Defects in SOX17 are the cause of vesicoureteral reflux type 3 (VUR3) [MIM:613674]. VUR3 is a disease belonging to the group of congenital anomalies of the kidney and urinary tract. It is characterized by the reflux of urine from the bladder into the ureters and sometimes into the kidneys, and is a risk factor for urinary tract infections. Primary disease results from a developmental defect of the ureterovesical junction. In combination with intrarenal reflux, the resulting inflammatory reaction may result in renal injury or scarring, also called reflux nephropathy. Extensive renal scarring impairs renal function and may predispose patients to hypertension, proteinuria, renal insufficiency and end-stage renal disease.
Similarity : Contains 1 HMG box DNA-binding domain.
Contains 1 Sox C-terminal domain.
Database links : UniProtKB/Swiss-Prot: Q9H6I2.1
英文名称 Anti-SNX5
中文名称 分选连接蛋白5抗体
别 名 0910001N05Rik; 1810032P22Rik; AU019504; D2Ertd52e; FLJ10931; OTTHUMP00000030340; OTTHUMP00000062927; OTTMUSP00000003367; OTTMUSP00000003368; RP11-504H3.2; RP23-35E16.2; snoRNA MBI-43; SNX 5; SNX5; SNX5_HUMAN; Sorting nexin 5; Sorting nexin-5.
浓 度 1mg/1ml
规 格 0.2ml/200μg
抗体来源 Rabbit
克隆类型 polyclonal
