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Rabbit Anti-ANKLE2 antibody
多克隆  |   SKU:bs-9743R

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货号:bs-3351R
¥1280
订购号:bs-9743R
¥1138.00-2900.00
货期:现货
Rabbit Anti-ANKLE2 antibody
反应物种(预测)

Rat,Cow,Horse,Rabbit,Sheep

产品应用(已验证)

WB

产品应用(可尝试)

IHC,IF,ELISA

推荐稀释比例

WB=1:500-2000,Elisa=1:5000-10000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:50-200,

研究领域

细胞生物,免疫学

标签

Array

  • Sample:
    HepG2(Human) Cell Lysate at 30 ug
    Molt-4Human) Cell Lysate at 30 ug
    HL60(Human) Cell Lysate at 30 ug
    A431(Human) Cell Lysate at 30 ug
    A549(Human) Cell Lysate at 30 ug
    Cerebrum (Mouse) Lysate at 40 ug
    Stomach (Mouse) Lysate at 40 ug
    Lung (Mouse) Lysate at 40 ug
    Spleen (Mouse) Lysate at 40 ug
    Heart (Mouse) Lysate at 40 ug
    Primary: Anti-ANKLE2 (bs-9743R) at 1/1000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 117 kD
    Observed band size: 117 kD

产品信息

RRID:RRID
产品名称:Rabbit Anti-ANKLE2 antibody
别名: ANKL2_HUMAN; ANKLE 2; ANKLE2; ankyrin repeat and LEM domain containing 2; Ankyrin repeat and LEM domain-containing protein 2; LEM domain containing 7; LEMD 7; LEMD7.
中文名称:ANKLE2蛋白抗体
英文名称:Rabbit Anti-ANKLE2 antibody
抗体来源: Rabbit
克隆类型:多克隆
细胞定位:细胞浆,细胞膜
性 状:Liquid
亚 型:IgG
纯化方法:affinity purified by Protein A
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

免疫原信息

免 疫 原:KLH conjugated synthetic peptide derived from human ANKLE2
抗原表位:251-350/938
SWISS:Q86XL3
Gene ID :23141
Human Gene ID:23141

产品介绍

Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKLE2 (ankyrin repeat and LEM domain containing 2), also known as LEMD7, is a 938 amino acid single-pass membrane protein containing an ANK repeat and a LEM domain. Exsiting as two isoforms produced by alternative splicing events, the gene encoding ANKLE2 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Function:Involved in mitotic nuclear envelope reassembly by promoting dephosphorylation of BAF/BANF1 during mitotic exit. Coordinates the control of BAF/BANF1 dephosphorylation by inhibiting VRK1 kinase and promoting dephosphorylation of BAF/BANF1 by protein phosp
Subunit:Interacts with BAF/BANF1. Interacts with protein phosphatase 2A (PP2A) components PPP2C (PPP2CA or PPP2CB) and PPP2R1A.
Subcellular Location:Endoplasmic reticulum membrane; Single-pass type III membrane protein.
Similarity:Belongs to the ANKLE2 family.
Contains 1 ANK repeat.
Contains 1 LEM domain.
Important Note:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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