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           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
国产精品扒开腿做爽爽爽视频 ,中文字幕无码视频
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
HAX1 Rabbit pAb (bs-7626R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產(chǎn)品編號 bs-7626R
英文名稱 HAX1 Rabbit pAb
中文名稱 造血干細胞特異性相關(guān)結(jié)合蛋白1抗體
別    名 HAX 1; Hax1a; HCLS1 and PKD2 associated protein; HCLS1 associated protein; HCLS1 associated protein X 1; HCLSBP1; HS 1 associated protein X 1; HS 1 binding protein; HS1 associating protein X 1; HS1 binding protein 1; HS1 binding protein; HS1BP1; SCN3.  
Specific References  (1)     |     bs-7626R has been referenced in 1 publications.
[IF=3.038] Jiajia Chenet al. Novel Role of HAX-1 in Neurons Protection After Spinal Cord Injury Involvement of IRE-1. Neurochem Res . 2020 Oct;45(10):2302-2311.  WB, IHC ;  rat.  
研究領(lǐng)域 細胞生物  細胞凋亡  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Dog,Horse)
產(chǎn)品應(yīng)用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 31 kDa
檢測分子量
細胞定位 細胞核 細胞漿 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human HAX1: 191-279/279 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ 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(chǎn)品介紹 RelevanceHAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.

Function:
Promotes cell survival. Potentiates GNA13-mediated cell migration. Involved in the clathrin-mediated endocytosis pathway. May be involved in internalization of ABC transporters such as ABCB11. May inhibit CASP9 and CASP3. May regulate intracellular calcium pools.

Subunit:
Interacts with ABCB1, ABCB4 and ABCB11 (By similarity). Directly associates with HCLS1/HS1, through binding to its N-terminal region. Interacts with CTTN. Interacts with PKD2. Interacts with GNA13. Interacts with CASP9. Interacts with ITGB6. Interacts with PLN and ATP2A2; these interactions are inhibited by calcium. Interacts with GRB7. Interacts (via C-terminus) with XIAP/BIRC4 (via BIR 2 domain and BIR 3 domain) and this interaction blocks ubiquitination of XIAP/BIRC4.

Subcellular Location:
Mitochondrion. Endoplasmic reticulum. Nucleus membrane. Cytoplasmic vesicle (By similarity). Sarcoplasmic reticulum (By similarity).

Tissue Specificity:
Ubiquitous. Up-regulated in oral cancers.

Post-translational modifications:
Proteolytically cleaved by caspase-3 during apoptosis.

DISEASE:
Defects in HAX1 are the cause of neutropenia severe congenital autosomal recessive type 3 (SCN3) [MIM:610738]; also known as Kostmann disease. A disorder of hematopoiesis characterized by maturation arrest of granulopoiesis at the level of promyelocytes with peripheral blood absolute neutrophil counts below 0.5 x 10(9)/l and early onset of severe bacterial infections. Some patients affected by severe congenital neutropenia type 3 have neurological manifestations such as psychomotor retardation and seizures. Note=The clinical phenotype due to HAX1 deficiency appears to depend on the localization of the mutations and their influence on the transcript variants. Mutations affecting exclusively isoform 1 are associated with isolated congenital neutropenia, whereas mutations affecting both isoform 1 and isoform 5 are associated with additional neurologic symptoms.

Similarity:
Belongs to the HAX1 family.

Gene ID:
10456

HAX1蛋白在線粒體蛋白廣泛表達,是一種抗凋亡蛋白,與bel-2有相似的機制。
版權(quán)所有 2004-2026 m.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: 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
精品國產亂子倫一區二區 | 高清无码一区二区三区四区 | av免费在线观看网站 | 亞洲五十路無碼亂倫 | 亚洲一区二区在线 | 国产suv精品一区二区69 | 免费毛片视频在线播放 | 婬妇BBW搡BBBB搡BBBB | 少妞躁BBB少妞躁BBBB | 国产suv精品一区二区69 | 四川少妇BBBBBB爽爽小说 | 国产一区二区三区免费观看 | 国产丰满熟妇蜜臀AV高潮 | 把女人弄爽A片一区免费 | 91久久爽久久爽爽久久片 | 国产BBB搡BBB爽爽爽 | 免费无套内谢少妇毛片A片软三 | 亚洲精品一区二区三区中文字幕 | 成人免费A片 喷 | 人妻日韩精品中文字幕 | 成人精品毛片内射视频 | AV 无码 高潮3满十八 | 精品人妻无码一区二区三区蜜桃一 | 国产老熟女高潮毛片A片仙踪林 | 久久久久成人精品免费播放动漫 | 无码中文AV一区二区三巨 | 国产精品va无码一区二区臀 | 国产精品免费一区二区 | 日日噜噜噜夜夜爽爽狠狠 | 西西人体44www大胆无码 | 国产69久久久欧美一级 | 久久精品一区二区三区四区 | 精品人妻少妇嫩草AV | 精品国产Av无码久久久影音先锋 | 91精品人妻熟女毛片A片骨灰盒 | 久久婷婷五月综合色国产香蕉 | 免费无码婬片AAAA片在线蜜芽 | 国产婬乱片A片AAA毛片下载 | 熟女高潮一区二区 | 寡妇高潮一级毛片免费 | 蜜桃AV噜噜噜一区二区 |