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ACAT1 抗体 (Middle Region)

This 兔 多克隆 anti-ACAT1 antibody specifically detects ACAT1 in WB 和 IHC. The antibody is reactive with 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔 和 斑马鱼 samples.
产品编号 ABIN2785629
发货至: 中国
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Quick Overview for ACAT1 抗体 (Middle Region) (ABIN2785629)

抗原

See all ACAT1 抗体
ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

适用

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人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼

宿主

  • 74
  • 7
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克隆类型

  • 62
  • 23
多克隆

标记

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This ACAT1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

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    Middle Region

    序列

    SYTRSKAAWE AGKFGNEVIP VTVTVKGQPD VVVKEDEEYK RVDFSKVPKL

    预测反应

    Cow: 93%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 86%

    产品特性

    This is a rabbit polyclonal antibody against ACAT1. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human ACAT1
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 427 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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 freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

    别名

    ACAT1

    背景

    ACAT1 is a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. The gene encoding ACAT1 spans approximately 27 kb and contains 12 exons interrupted by 11 introns. Defects in this gene are associated with the alpha-methylacetoaceticaciduria disorder, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. This gene spans approximately 27 kb and contains 12 exons interrupted by 11 introns. Defects in this gene are associated with the alpha-methylacetoaceticaciduria disorder, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
    Alias Symbols: ACAT, MAT, T2, THIL
    Protein Interaction Partner: SUMO2, MDM2, ACAT1, VCAM1, ITGA4, AGXT, FLOT1, UBAP2L, TTF2, UBL4A, UQCRFS1P1, UQCRB, SSBP1, SDHB, SDHA, SAFB, MARS, FOXM1, CSE1L, ACO2, TMEM65, TUBB1, TOMM7, TOPBP1, GCN1L1, TIMM44, ACAA2, FBXO6, PEX7, COPS5, CUL1, CUL3, SIRT7, SUMO1, RAD21, UBC, HDAC5,
    Protein Size: 427

    分子量

    41 kDa

    基因ID

    38

    NCBI登录号

    NM_000019, NP_000010

    UniProt

    P35610
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