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BCAT1 抗体 (Middle Region)
BCAT1
适用: 人
WB, IHC (p), EIA
宿主: 兔
Polyclonal
unconjugated
BCAT1抗体详情
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抗原
See all BCAT1 抗体
BCAT1
(Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))
抗原表位
All epitopes for BCAT1 抗体
AA 88-115, Middle Region
适用
All reactivities for BCAT1 抗体
人
宿主
All hosts for BCAT1 抗体
兔
克隆类型
All clonalities for BCAT1 抗体
多克隆
标记
All conjugates for BCAT1 抗体
This BCAT1 antibody is un-conjugated
应用范围
All applications for BCAT1 抗体
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
特异性
This antibody reacts to BCAT1.
交叉反应 (详细)
Species reactivity (tested):Human.
纯化方法
Affinity chromatography on Protein A
免疫原
KLH conjugated synthetic peptide between 88-115 amino acids from the Central region of human BCAT1
亚型
Ig Fraction
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Discover our top product BCAT1 Primary Antibody
Alternatives
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使用细节
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应用备注
Optimal working dilution should be determined by the investigator.
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
0.25 mg/mL
缓冲液
PBS containing 0.09 % (W/V) sodium azide as preservative
储存液
Sodium azide
注意事项
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
注意事项
Avoid repeated freezing and thawing.
储存条件
4 °C/-20 °C
储存方法
Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
BCAT1目标详情
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抗原
BCAT1
(Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))
别名
BCAT1 (BCAT1 产品 )
别名
fj66g02 antibody, zgc:73157 antibody, wu:fj66g02 antibody, Bcatc antibody, BCATC antibody, BCT1 antibody, ECA39 antibody, MECA39 antibody, PNAS121 antibody, PP18 antibody, BCATc antibody, Eca39 antibody, branched chain amino-acid transaminase 1, cytosolic antibody, branched chain amino acid transaminase 1 antibody, branched chain amino-acid transaminase 1, cytosolic L homeolog antibody, branched chain aminotransferase 1, cytosolic antibody, bcat1 antibody, BCAT1 antibody, bcat1.L antibody, Bcat1 antibody
背景
This gene encodes the cytosolic form of the enzyme branched-chain amino acid transaminase. This enzyme catalyzes the reversible transamination of branched-chain alpha-keto acids to branched-chain L-amino acids essential for cell growth. Two different clinical disorders have been attributed to a defect of branched-chain amino acid transamination: hypervalinemia and hyperleucine-isoleucinemia. As there is also a gene encoding a mitochondrial form of this enzyme, mutations in either gene may contribute to these disorders. Alternatively spliced transcript variants have been described.Synonyms: BCAT(c), BCT1, Branched-chain-amino-acid aminotransferase cytosolic, ECA39
基因ID
586
NCBI登录号
NP_001171562
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