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FAM134A Rabbit pAb (bs-14725R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-14725R
英文名稱 FAM134A Rabbit pAb
中文名稱 FAM134A蛋白抗體
別    名 C2orf17; F133B_HUMAN; FAM134A family with sequence similarity 134, member A.  
Specific References  (1)     |     bs-14725R has been referenced in 1 publications.
[IF=4.85] Yutong Wu. et al. Osteoclast-derived extracellular miR-106a-5p promotes osteogenic differentiation and facilitates bone defect healing. CELL SIGNAL. 2022 Dec;:110549  IHC ;  Mouse.  
研究領域 細胞生物  信號轉導  轉運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Human
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,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 58 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FAM134A 
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
產品介紹 The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FAM134A gene product has been provisionally designated FAM134A pending further characterization.

Function:
The function of this protein remains unknown.

Subcellular Location:
Membrane; Multipass membrane protein.

Similarity:
Belongs to the FAM133 family.

SWISS:
Q8NC44

Gene ID:
79137

Database links:

Entrez Gene: 79137 Human

Entrez Gene: 227298 Mouse

Entrez Gene: 363252 Rat

NCBI: NP_077269 Human

SwissProt: Q8NC44 Human

SwissProt: Q6NS82 Mouse

SwissProt: Q3MHU5 Rat



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