强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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(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
国产精品嫩草AV城中村,婬荡欲女搡BBBB搡BBB视频
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-SPTLC1/Cy5.5 Conjugated antibody (bs-4087R-Cy5.5)
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  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-4087R-Cy5.5
英文名稱 Rabbit Anti-SPTLC1/Cy5.5 Conjugated antibody
中文名稱 Cy5.5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(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, )
產(chǎn)品應(yīng)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.nmgps.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
快日啊爽快视频交换草穴刺激欧美激情 | 少妇做爰高潮免费看片 | 国内外成人激情视频在线 | 亚洲无码精品一区二区 | 台湾天天成人综合娱乐网 | 狠狠人妻久久久久久综合蜜桃 | 国产妓女精品一区二区 | 强伦人妻一区二区三区 | 91午夜人妻人人做人爽 | 野性猛交ⅩXXX乱大交 | 中文字幕一区成人电影 | 日韩精品无码一区二区 | 国产精品午夜未成人免费观看 | 午夜理理伦A片在线播放 | 红桃视频网站一区二区精品 | 亚洲女人天堂成人AV在线 | 蜜桃秘 无码一线二线三线av | 特级西西www大胆无码 | 国产乱人偷精品人妻A片免费网址 | 国产丝袜美女在线观看 | 免费无码婬片AA片按摩 | 人妻激情综合久久久久 | 亚洲无码淫荡人妻对白 | 日本三级片免费观看网站 | 四川寡妇搡BBB爽爽爽 | 亚洲va在线观看 | 日本免费三 片免费观看 | 同性无码A片在线观看 | 亚洲中文字幕在线播放 | 中文字幕在线免费视频 | 黄色视频免费观看无码 | 93人妻人人揉人人躁人人 | 免费黄色视频网站在线看 | 午夜高清无码在线观看 | 午夜无码人妻AⅤ大片大象传媒 | 亚洲AV蜜桃臀永久无码精品无码 | 在线观看成人免费视频 | 蜜桃臀大屁股无码视频 | renrencao超碰| 熟妇中出映像近相奸熟妇 | 国产精品美女操逼 |