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
漂亮少妇高潮A片XXXX,,国产乱人伦无码视频
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-HAX1/BF488 Conjugated antibody (bs-7626R-BF488)
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-7626R-BF488
英文名稱 Rabbit Anti-HAX1/BF488 Conjugated antibody
中文名稱 BF488標記的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.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
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 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, )
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 31kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human HAX1
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:
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.

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

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 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
国产午夜影院福利区 | 17c.com一起草久久久网站 | 黄色免费在线观看视频 | 一区少妇白洁无码视频 | 蜜桃AV一区二区精品无码 | 99人妻碰碰碰久久久久禁片 | 波多野结衣精品一区二区 | 亚洲精品无码成人片久久-涡桑剁 | 日本中文字幕爱丝袜 | 国产伦精一区二区三赶尸艳谈 | 二三级成人夜晚观看视频 | 欧美久久17c一区二区 | 亚洲AV无码乱码精品国产白浆 | 日本丰满少妇一区二区三区 | 日本无码人妻波多野结衣杨思敏 | 狠狠人妻久久久久久综合99浪潮 | 内捧疯狂进出免费视频 | 无码人妻一区二区三区免费九色 | 蜜桃视频com.www | 国产超碰人人做人人爽 | 高清无码视频在线播放 | 亚洲日韩在线视频 | 亚洲国产成人精品无码区6080 | 一区二区欧美xxBB | 国产99视频在线观看 | 中国BBBBBBBBB毛毛 | 啊啊亚洲无吗视频免费 | 影音先锋女人aV鲁色资源网站 | 海角国产真实交换配乱 | 婷婷99狠狠躁天天躁中文字幕 | 黄色视频在线观看无码免费 | 国产毛片AAAAA级 | 亚洲精品一区二区三区四区高清 | 99成人乱码一区二区三区网站 | 人超人碰人摸免费视频 | 精品无码视频在线免费观看 | 亚洲日韩精品视频在线 | 美女裸体洗澡A片免费看 | 亚洲无码中文字幕国产 | 国产伦子伦视频免费播放 | 国产美女无遮挡裸永久观看 |