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Rabbit Anti-Complement component C9b antibody
多克隆  |   SKU:bs-15307R

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货号:bs-3351R
¥1280
订购号:bs-15307R
¥1098.00-2900.00
货期:现货
Rabbit Anti-Complement component C9b antibody
反应物种(预测)

Mouse,Rat,Dog,Pig,Cow,Sheep

产品应用(已验证)

WB,FCM

产品应用(可尝试)

ELISA

推荐稀释比例

WB=1:500-2000,Elisa=1:5000-10000,Flow Cyt=1ug/Test,

研究领域

细胞生物,免疫学

标签

Array

  • Blank control: HL60.
    Primary Antibody (green line): Rabbit Anti-Complement component C9b antibody (bs-15307R)
    Dilution: 1μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-PE
    Dilution: 1μg /test.
    Protocol
    The cells then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
  • Sample:
    Lane 1: Human Jurkat cell lysates
    Lane 2: Human HL-60 cell lysates
    Primary: Anti-Complement component C9b (bs-15307R) at 1/1000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 32/61 kDa
    Observed band size: 61 kDa
  • Black line : Positive blank control (HL60); Negative blank control (A431)
    Green line : Primary Antibody (Rabbit Anti-C9b antibody (bs-15370R) )
    Orange line:Isotype Control Antibody (Rabbit IgG) .
    Blue line : Secondary Antibody (Goat anti-rabbit IgG-PE)/(Goat anti-rabbit IgG-AF488)
    HL60(Positive)and A431(Negative control)cells (black) were incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with C9b Antibody(bs-15307R)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2% BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).

产品信息

RRID:RRID
产品名称:Rabbit Anti-Complement component C9b antibody
别名: C9b; CO9_HUMAN; Complement component C9; Complementcomponent C9b.
中文名称:补体C9b抗体
英文名称:Rabbit Anti-Complement component C9b antibody
抗体来源: Rabbit
克隆类型:多克隆
细胞定位:细胞膜,分泌型蛋白
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 Complementcomponent C9b
抗原表位:251-350/559
SWISS:P02748
Gene ID :735
Human Gene ID:735

产品介绍

C9 is a plasma protein synthesized in the liver and monocytes consisting of a single polypeptide chain. C9 is a part of the membrane attack complex (MAC), an important component of the immune system. The MAC forms upon complement system activation by invading pathogenic bacteria and consists of the four major complement proteins: C5b, C6, C7 and C8. These complement proteins bind to the outer surface of the plasma membrane of the invading cell. C9 binds to the membrane associated C5b-8 protein, which leads to the circular polymerization of 12-18 C9 molecules. These polymerized C9 molecules form a ring structure in the membrane. Molecules can then diffuse freely through this transmembrane channel, causing cell lysis and destruction of the invading bacterial cell.
Function:Constituent of the membrane attack complex (MAC) that plays a key role in the innate and adaptive immune response by forming pores in the plasma membrane of target cells. C9 is the pore-forming subunit of the MAC.
Subunit:Component of the membrane attack complex (MAC). MAC assembly is initiated by protelytic cleavage of C5 into C5a and C5b. C5b binds sequentially C6, C7, C8 and multiple copies of the pore-forming subunit C9.
Subcellular Location:Secreted. Cell membrane; Multi-pass membrane protein. Note=Secreted as soluble monomer. Oligomerizes at target membranes, forming a pre-pore. A conformation change then leads to the formation of a 100 Angstrom diameter pore.
Tissue Specificity:Plasma.
Post-translational modifications:Thrombin cleaves factor C9 to produce C9a and C9b.
Phosphorylation sites are present in the extracellular medium.
DISEASE:Defects in C9 are a cause of complement component 9 deficiency (C9D) [MIM:613825]. A rare defect of the complement classical pathway associated with susceptibility to severe recurrent infections, predominantly by Neisseria gonorrhoeae or Neisseria meningi
Similarity:Contains 1 EGF-like domain.
Contains 1 LDL-receptor class A domain.
Contains 1 MACPF domain.
Contains 1 TSP type-1 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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