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GLA 抗体 (N-Term)

This anti-GLA antibody is a 兔 多克隆 antibody detecting GLA in WB. Suitable for 人, 小鼠, 大鼠, 犬, 豚鼠, 马, Cow, 山羊, 兔 和 斑马鱼.
产品编号 ABIN2785641
发货至: 中国

Quick Overview for GLA 抗体 (N-Term) (ABIN2785641)

抗原

See all GLA 抗体
GLA (Galactosidase, alpha (GLA))

适用

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人, 小鼠, 大鼠, 犬, 豚鼠, 马, Cow, 山羊, 兔, 斑马鱼

宿主

  • 102
  • 18
  • 2

克隆类型

  • 94
  • 28
多克隆

标记

  • 64
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This GLA antibody is un-conjugated

应用范围

  • 86
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  • 13
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  • 6
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Western Blotting (WB)
  • 抗原表位

    • 16
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    • 8
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    • 4
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    N-Term

    序列

    PQRFPHGIRQ LANYVHSKGL KLGIYADVGN KTCAGFPGSF GYYDIDAQTF

    预测反应

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

    产品特性

    This is a rabbit polyclonal antibody against GLA. 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 N terminal region of human GLA
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 429 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

    GLA (Galactosidase, alpha (GLA))

    别名

    GLA

    背景

    GLA is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. 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: GALA
    Protein Interaction Partner: ZNF622, CNDP2, MAT2B, EIF4H, PGD, GNS, GBP2, G6PD, EIF5, CAPN1, ALDH7A1, TERT, UBC, FBXO6, OTUD4, GLA,
    Protein Size: 429

    分子量

    45 kDa

    基因ID

    2717

    NCBI登录号

    NM_000169, NP_000160

    UniProt

    P06280

    途径

    SARS-CoV-2 Protein Interactome
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