SAB4300571
Anti-MAP1LC3A antibody produced in rabbit
affinity isolated antibody
别名:
Anti-LC3 antibody produced in rabbit, Anti-LC3A antibody produced in rabbit, Anti-MAP1ALC3 antibody produced in rabbit, Anti-MAP1BLC3 antibody produced in rabbit, Anti-microtubule-associated protein 1 light chain 3 alpha antibody produced in rabbit
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所有图片(2)
About This Item
分類程式碼代碼:
12352203
NACRES:
NA.41
推荐产品
生物源
rabbit
品質等級
共軛
unconjugated
抗體表格
affinity isolated antibody
抗體產品種類
primary antibodies
無性繁殖
polyclonal
形狀
buffered aqueous solution
分子量
~16 kDa
~18 kDa
物種活性
rat, human, mouse
濃度
1 mg/mL
技術
indirect immunofluorescence: 1:100-1:200
western blot: 1:500-1:1000
同型
IgG
免疫原序列
(R-P-F-K-Q)
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
儲存溫度
−20°C
目標翻譯後修改
unmodified
基因資訊
human ... MAP1LC3A(84557)
免疫原
Peptide sequence around aa. 5-10 (R-P-F-K-Q), according to the protein MAP1LC3A.
特點和優勢
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.
標靶描述
Probably involved in formation of autophagosomal vacuoles (autophagosomes).
外觀
Solution in phosphate-buffered saline containing 0.02% sodium azide and 50% glycerol
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Bing Han et al.
Experimental and therapeutic medicine, 22(4), 1054-1054 (2021-08-27)
Human respiratory syncytial virus (RSV) is a major health challenge due to the lack of a safe and effective vaccine and antiviral drugs. RSV non-structural protein 1 (NS1) is the main inhibitor of antiviral signaling pathways in RSV infection; however
Antonio Piras et al.
Cell death & disease, 8(12), 3223-3223 (2017-12-21)
Spinal muscular atrophy (SMA) is a recessive autosomal neuromuscular disease, due to homozygous mutations or deletions in the telomeric survival motoneuron gene 1 (SMN1). SMA is characterized by motor impairment, muscle atrophy, and premature death following motor neuron (MN) degeneration.
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