吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務
  
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  人才招聘  關(guān)于我們  聯(lián)系我們
香蕉久久精品日日躁夜夜躁,日本少妇又色又爽又高潮,14表妺好紧没带套18分钟
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-SPTLC1/Cy3 Conjugated antibody (bs-4087R-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-4087R-Cy3
英文名稱1 Rabbit Anti-SPTLC1/Cy3 Conjugated antibody
中文名稱 Cy3標記的絲氨酸棕櫚酰轉(zhuǎn)移酶1抗體
別    名 HSAN; HSAN1; HSN1; LBC1; LCB 1; LCB1; Long chain base biosynthesis protein 1; Serine C palmitoyltransferase; Serine palmitoyl CoA transferase 1; Serine palmitoyltransferase 1; Serine palmitoyltransferase long chain base subunit 1; Serine palmitoyltransferase subunit 1; SPT 1; SPT1; SPTI; SPTLC 1; SPTC1_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 腫瘤  心血管  免疫學  染色質(zhì)和核信號  神經(jīng)生物學  信號轉(zhuǎn)導  細胞凋亡  轉(zhuǎn)錄調(diào)節(jié)因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, )
產(chǎn)品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 53kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SPTLC1
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 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.
產(chǎn)品介紹 background:
This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013]

Function:
Serine palmitoyltransferase (SPT). The heterodimer formed with SPTLC2 or SPTLC3 constitutes the catalytic core. The composition of the serine palmitoyltransferase (SPT) complex determines the substrate preference. The SPTLC1-SPTLC2-SPTSSA complex shows a strong preference for C16-CoA substrate, while the SPTLC1-SPTLC3-SPTSSA isozyme uses both C14-CoA and C16-CoA as substrates, with a slight preference for C14-CoA. The SPTLC1-SPTLC2-SPTSSB complex shows a strong preference for C18-CoA substrate, while the SPTLC1-SPTLC3-SPTSSB isozyme displays an ability to use a broader range of acyl-CoAs, without apparent preference.

Subunit:
Heterodimer with SPTLC2 or SPTLC3. Component of the serine palmitoyltransferase (SPT) complex, composed of SPTLC1, either SPTLC2 or SPTLC3, and either SSSPTA or SSSPTB. Interacts with SPTSSA and SPTSSB; the interaction is direct. Interacts with ORMDL3.

Subcellular Location:
Endoplasmic reticulum membrane; Single-pass membrane protein

Tissue Specificity:
Widely expressed. Not detected in small intestine.

DISEASE:
Defects in SPTLC1 are the cause of hereditary sensory and autonomic neuropathy type 1A (HSAN1A) [MIM:162400]. The hereditary sensory and autonomic neuropathies are a genetically and clinically heterogeneous group of disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and by sensory and/or autonomic abnormalities. HSAN1A is an autosomal dominant axonal neuropathy with onset in the second or third decades. Initial symptoms are loss of pain, touch, heat, and cold sensation over the feet, followed by distal muscle wasting and weakness. Loss of pain sensation leads to chronic skin ulcers and distal amputations.

Similarity:
Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family.

Database links:

Entrez Gene: 426145 Chicken

Entrez Gene: 739412 Chimpanzee

Entrez Gene: 614165 Cow

Entrez Gene: 100726468 Guinea pig

Entrez Gene: 10558 Human

Entrez Gene: 268656 Mouse

Entrez Gene: 100344536 Rabbit

Entrez Gene: 705324 Rhesus monkey

Omim: 605712 Human

SwissProt: Q3MHG1 Cow

SwissProt: Q60HD1 Cynomolgus Monkey

SwissProt: O15269 Human

SwissProt: O35704 Mouse

Unigene: 90458 Human

Unigene: 240336 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.xucheq.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: 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: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網(wǎng)安備110107000727號
国产精品久久久久av| 西班牙女郎完整版在线播放 | 最近高清中文在线字幕在线观看| 亚洲精品国偷拍自产在线观看蜜臀| 国产99在线 | 亚洲| 天天躁人人躁人人躁狂躁 | 无码人妻一区二区三区精品视频| 88国产精品视频一区二区三区| 女公务员人妻呻吟求饶| 国产精品无码久久久久| 欧美日韩午夜群交多人轮换| 久久久婷婷五月亚洲97号色| 中文字幕亚洲乱码熟女一区二区| 嗯快点别停舒服好爽受不了了| 婷婷开心激情综合五月天| 无码精品人妻一区二区三区AV| 无码国产精成人午夜视频一区二区| 日本JAPANESE丰满少妇| 黑人猛挺进小莹的体内视频| 精品久久久久久亚洲综合网| 无码人妻久久一区二区三区蜜桃| 国产SUV精品一区二人妻| 水蜜桃AV无码| 一本一道AV无码中文字幕| 久久久久久久97| 国产AV无码专区亚洲AV毛片搜| 免费男人下部进女人下部视频| 精品久久欧美熟妇WWW| CHINA中国妞TUBESEX| 国产福利视频| 永久黄网站色视频免费直播 | 国产99久久久国产精品~~牛| 久久久无码精品亚洲日韩按摩| 亚洲AV永久中文无码精品综合| 少妇性饥渴姓交HDSEX| 午夜福利理论片在线观看| 国产999精品久久久久久| 日韩乱码人妻无码中文字幕| av片在线观看免费| 无码国产精成人午夜视频一区二区| 脱岳裙子从后面挺进去视频|