mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
99热国产在线手机精品99,亚洲在线av一区二区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ACTG1/Gold Conjugated antibody (bs-10968R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@www.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.p2b3.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-10968R-Gold
英文名稱 Rabbit Anti-ACTG1/Gold Conjugated antibody
中文名稱 膠體金標記的肌動蛋白γ1抗體
別    名 ACT; ACTB; ACTG; ACTG_HUMAN; actg1; Actin, cytoplasmic 2; Actin, gamma 1; Actin, gamma 1 propeptide; cytoplasmic 2; Cytoskeletal gamma actin; Deafness, autosomal dominant 20; Deafness, autosomal dominant 26; DFNA20; DFNA26; N-terminally processed.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 信號轉導  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應
產品應用 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 42kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ACTG1
亞    型 IgG
純化方法 affinity purified by Protein A
儲 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.
產品介紹 background:
Actins are highly conserved proteins that are involved in various types of cell motility, and maintenance of the cytoskeleton. In vertebrates, three main groups of actin isoforms, alpha, beta and gamma have been identified. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton, and as mediators of internal cell motility. Actin, gamma 1, encoded by this gene, is a cytoplasmic actin found in non-muscle cells. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]

Function:
Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.

Subunit:
Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others.

Subcellular Location:
Cytoplasm, cytoskeleton.

Post-translational modifications:
The methylhistidine determined by Bienvenut et al is assumed to be the tele-methylhistidine isomer by similarity to the mouse ortholog.
Oxidation of Met-44 and Met-47 by MICALs (MICAL1, MICAL2 or MICAL3) to form methionine sulfoxide promotes actin filament depolymerization. MICAL1 and MICAL2 produce the (R)-S-oxide form. The (R)-S-oxide form is reverted by MSRB1 and MSRB2, which promote actin repolymerization.
Monomethylation at Lys-84 (K84me1) regulates actin-myosin interaction and actomyosin-dependent processes. Demethylation by ALKBH4 is required for maintaining actomyosin dynamics supporting normal cleavage furrow ingression during cytokinesis and cell migration.

DISEASE:
Deafness, autosomal dominant, 20 (DFNA20) [MIM:604717]: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. Note=The disease is caused by mutations affecting the gene represented in this entry.
Baraitser-Winter syndrome 2 (BRWS2) [MIM:614583]: A rare developmental disorder characterized by the combination of congenital ptosis, high-arched eyebrows, hypertelorism, ocular colobomata, and a brain malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short stature and microcephaly, intellectual disability, seizures, and hearing loss. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the actin family.

Database links:

Entrez Gene: 415296 Chicken

Entrez Gene: 71 Human

Entrez Gene: 11465 Mouse

Entrez Gene: 100361457 Rat

Entrez Gene: 287876 Rat

Entrez Gene: 57935 Zebrafish

Omim: 102560 Human

SwissProt: Q5ZMQ2 Chicken

SwissProt: P63261 Human

SwissProt: P63260 Mouse

SwissProt: P63259 Rat

SwissProt: Q7ZVF9 Zebrafish

Unigene: 514581 Human

Unigene: 196173 Mouse

Unigene: 426706 Mouse

Unigene: 101464 Rat

Unigene: 106826 Rat

Unigene: 155448 Zebrafish



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.www.p2b3.cn 北京博奧森生物技術有限公司
通過國際質量管理體系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         京公網安備110107000727號
日韩久久奶茶视频| 一区二区三区中文字幕免费在线| 亚洲国产国产综合一区首页| 挺进绝色邻居的紧窄小肉| 亚洲 欧美 日韩 主播| 96精品久久久久久蜜臀浪| 国产综合精品一区二区青青| 波多野吉衣一区在线观看| 亚洲欧美一区二区三区孕妇| 精品一区二区三区成人免费视频| 性色av少妇一区二区三区多人| 日韩精品一区av在线| 中国熟女色av夜夜嗨| 中文字幕无码区一区二区| 美性中文网中文字幕91| 国产精品碰碰现在自| 欧美高清在线观看一区二区三区| 狂插美女大屁股在线观看| 被公侵犯人妻少妇一区二区三区| 午夜理论理论亚洲激情| 裸毛片视频在线视频| 在线免费观看一区二区三区| 人人妻人人澡精品99| 欧美黑屌操B内射冒白浆| 男人的下面进女人的下面在线观看| 日韩aaa成人免费观看| 国产一区二区三区午夜精品久久| 国产精品视频一区二区三区八戒| 国产日韩一区二区三区在线播放| 免费国产香蕉视频在线观看| 日韩欧美一区二三区风间由美| 欧美精品一区二区三区四区五区| 国产精品一区二区三区色噜噜| 高颜值美女视频在线观看| 大黑屌日本另类肛交| 国产精品538一区二区在线| 亚洲综合欧美日韩| 欧美一区二区三区四公司| 久久精品国产亚洲高清| 美女呻吟翘臀后进爆白浆| 日本韩国国产精品一区|