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FUNDC1 Rabbit pAb (bs-13227R)  
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50ul/1180.00元
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產(chǎn)品編號 bs-13227R
英文名稱 FUNDC1 Rabbit pAb
中文名稱 X三體綜合癥相關(guān)蛋白FUNDC1抗體
別    名 FUN14 domain containing protein 1; FUN14 domain-containing protein 1; FUND1_HUMAN.  
Specific References  (1)     |     bs-13227R has been referenced in 1 publications.
[IF=4.011] Xu G et al. Fundc1?is?necessary?for?proper?body?axis?formation?during?embryogenesis?in zebrafish. Sci Rep.?2019 Dec 11;9(1):18910.  WB ;  grass carp&Human.  
研究領(lǐng)域 細胞生物  免疫學  發(fā)育生物學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,Mouse,Rat
產(chǎn)品應用 WB=1:300-800,ICC/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 17 kDa
檢測分子量
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from mouse FUNDC1 
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 FUNDC1 is a 155 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC1 maps to human chromosome Xp11.3 and mouse chromosome X A1.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Function:
Acts as an activator of hypoxia-induced mitophagy, an important mechanism for mitochondrial quality control.

Subunit:
Interacts (via YXXL motif) with MAP1 LC3 family proteins MAP1LC3A, MAP1LC3B and GABARAP.

Subcellular Location:
Mitochondrion outer membrane; Multi-pass membrane protein.

Tissue Specificity:
Widely expressed.

Post-translational modifications:
Phosphorylation at Tyr-18 by SRC inhibits activation of mitophagy. Following hypoxia, dephosphorylated at Tyr-18, leading to interaction with MAP1 LC3 family proteins and triggering mitophagy.

Similarity:
Belongs to the FUN14 family.

SWISS:
Q9DB70

Gene ID:
72018

Database links:

Entrez Gene: 139341 Human

Entrez Gene: Mouse

Entrez Gene: 72018 Mouse

Entrez Gene: 363442 Rat

Omim: 300871 Human

SwissProt: Q8IVP5 Human

SwissProt: Q9DB70 Mouse

SwissProt: Q5BJS4 Rat



產(chǎn)品圖片
Sample: Lane 1: Mouse Cerebellum tissue lysates Lane 2: Mouse Heart tissue lysates Lane 3: Human 293T cell lysates Lane 4: Human MCF-7 cell lysates Lane 5: Human A549 cell lysates Primary: Anti-FUNDC1 (bs-13227R) at 1/800 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 17 kDa Observed band size: 17 kDa
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