91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
www.无码爆浆蜜桃.com,国产亲子乱婬一级A片
Rabbit Anti-GAD67/Gold Conjugated antibody (bs-1302R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-1302R-Gold
英文名稱 Rabbit Anti-GAD67/Gold Conjugated antibody
中文名稱 膠體金標(biāo)記的谷氨酸脫羧酶67抗體
別    名 glutamate decarboxylase 67; decarboxylase 1; 67 kDa glutamic acid decarboxylase; Glutamate decarboxylase 67 kDa isoform; GAD1; GAD; GAD-67; GAD 67.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul(10nm  15nm  35nm
研究領(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, )
產(chǎn)品應(yīng)用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 67kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GAD67
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
Glutamic Acid Decarboxylase (GAD) catalyzes the conversion of L glutamate to g-aminobutyric acid (GABA), the principal inhibitory neurotransmitter in the brain, and a putative paracrine signal molecule in pancreatic islets. GAD has a restricted tissue distribution. It is highly expressed in the cytoplasm of GABAergic neurons in the central nervous system (CNS) and pancreatic beta cells. It is also present in other non-neuronal tissues such as testis, oviduct and ovary. GAD is also transiently expressed in non-GABAergic cells of the embryonic and adult nervous system, suggesting its involvement in development and plasticity.
GAD exists as two isoforms, GAD65 and GAD67 (molecular masses of 65 and 67 kD, respectively) that are encoded by two different genes. GAD65 is an ampiphilic, membraneanchored protein, (585 amino acid residues) and is encoded on human chromosome 10. GAD67 is a cytoplasmic protein (594 amino acid residues) and is encoded on chromosome 2. There is 64% amino acid identity between the two isoforms, with the highest diversity located at the N terminus, which in GAD65 is required for targeting the enzyme to GABA-containing secretory vesicles. The two isoforms appear to have distinct intraneuronal distribution in the brain. GAD65 has been identified as an autoantigen in insulindependent diabetes mellitus (IDDM) and stiff-man syndrome (SMS), IDDM is an autoimmune disease that results from T cell mediated destruction of pancreatic insulin-secreting beta cells. Islet-reactive T cells and antibodies primarily to GAD65 (also named beta cell autoantigen) can be detected in peripheral blood of 80% of recent-onset IDD patients and in pre-diabetic high-risk subjects before onset of clinical symptoms. This suggests that GAD may be an important marker in the early stages of the disease. Also, autoantibodies to GAD65 and GAD67 are detected in animal models of IDDM, including the non-obese diabetes (NOD) mouse. In the NOD mouse, T cell reactivity is initially restricted to the C terminal regions of GAD65, but later spreads to other parts of GAD65. Stiff-man syndrome (SMS), a rare disorder of the CNS, is characterized by progressive rigidity of the body musculature with painful spasms, due to impairment of the GABAergic neurotransmission.

Function:
Catalyzes the production of GABA.

Tissue Specificity:
Isoform 3 is expressed in pancreatic islets, testis, adrenal cortex, and perhaps other endocrine tissues, but not in brain.

DISEASE:
Defects in GAD1 are the cause of cerebral palsy spastic quadriplegic type 1 (CPSQ1) [MIM:603513]. A non-progressive disorder of movement and/or posture resulting from defects in the developing central nervous system. Affected individuals manifest symmetrical, non-progressive spasticity and no adverse perinatal history or obvious underlying alternative diagnosis. Developmental delay, mental retardation and sometimes epilepsy can be part of the clinical picture.

Similarity:
Belongs to the group II decarboxylase family.

Database links:

Entrez Gene: 2571 Human

Entrez Gene: 14415 Mouse

Entrez Gene: 24379 Rat

Omim: 605363 Human

SwissProt: Q99259 Human

SwissProt: P48318 Mouse

SwissProt: P18088 Rat

Unigene: 420036 Human

Unigene: 272120 Mouse

Unigene: 91245 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

GAD67谷氨酸脫羧酶-67 是用于I II型糖尿病研究的很重要的蛋白。GAD67的大多數(shù)表位位于蛋白中部或C末端1/3蛋白,與GAD65有高度的同源性。
版權(quán)所有 2004-2026 rvdoil.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過國際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
亲子乱高潮1000部 | 99国产精品久久久久久久 | 国产乱子子伦精品视频 | 国产精品WWW久久久久久 | 日本午夜精品理论片A级app发布 | 躁BBB躁BBB躁BBBBBB| 亚洲一区高清无码 | 调教我的妺妺H肉yin荡视频 | 91人妻人人妻人人爽人人精品DVD | 午夜视频免费在线观看 | 真实的国产乱XXXX在线 | 林ゆな无码一区8MAV | 亚洲激情在线观看 | 搡BBBB搡BBB搡我瞎了 | 色情一级AA片免费观看 | 一级特黄aa大片欧美 | 久久播瑟瑟爱人妻熟女 | 潘金莲全黄—级A片性舒淇 亚洲午夜精品一区二区蜜桃 | 国产寡妇婬乱a毛片视频1 | 三级片在线观看网站网址大全 | 国产69精品久久久久久久久久久久 | 国产人妻精品区一区二区 | 国产人妻A片三毛片 | 高清免费播放一曲二曲三曲 | 国产又爽又黄无码无遮在线观看 | 久久久久久久久久久国产 | 国产在线观看国偷精品 | 特级西西人体大胆无码 | 少妇伦子伦精品无吗 | 国产av一区二区三区 | 亚洲天堂在线观看无码 | 色情一级AA片免费观看 | 亚洲高清无码在线观看 | 欧美鲁丝亚洲精品 | 国产三级一区二区三区在线观看 | 黄色av网站在线观看 | 亚洲AV无码A片在线观看蜜桃 | 国产真实乱人偷精品视频 | 国语露脸刺激高清AV | 国产精品揄拍一区二区 | 強暴女警AV正片一区二区三区 |