Anti-CLSTN1 antibody [JE48-81]

产品描述

Induces KLC1 association with vesicles and functions as a cargo in axonal anterograde transport. Complex formation with APBA2 and APP, stabilizes APP metabolism and enhances APBA2-mediated suppression of beta-APP40 secretion, due to the retardation of intracellular APP maturation. In complex with APBA2 and C99, a C-terminal APP fragment, abolishes C99 interaction with PSEN1 and thus APP C99 cleavage by gamma-secretase, most probably through stabilization of the direct interaction between APBA2 and APP. The intracellular fragment AlcICD suppresses APBB1-dependent transactivation stimulated by APP C-terminal intracellular fragment (AICD), most probably by competing with AICD for APBB1-binding. May modulate calcium-mediated postsynaptic signals (By similarity).

产品名称Anti-CLSTN1 antibody [JE48-81]

分子量Predicted band size: 110 kDa.

种属反应性Human, Mouse

验证应用WB,IHC-P

抗体类型重组兔单抗

免疫原Recombinant protein within human CLSTN1 aa 881-981 (Cytoplasmic).

偶联Non-conjugated

性能

形态Liquid

浓度1 mg/mL.

存放说明Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.

存储缓冲液1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

亚型IgG

纯化方式Protein affinity purified.

亚细胞定位Endoplasmic reticulum. Golgi apparatus. Membrane. Nucleus.

数据链接SwissProt: O94985 Human

SwissProt: Q9EPL2 Mouse

其它名称

Alc alpha antibody

Alc-alpha antibody

Alcadein alpha 1 antibody

more

应用

• WB: 1:1000-1:5000
  IHC-P: 1:50-1:200

• 

  Fig1: Western blot analysis of CLSTN1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody  was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
  Positive control:
  Lane 1: Mouse brain tissue lysate
  Lane 2: Siha cell lysate
  Lane 3: Mouse cerebellum tissue lysate
  Lane 4: A431 cell lysate

  

  Fig2: Immunohistochemical analysis of paraffin-embedded human liver cancer tissue using anti-CLSTN1 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibodyfor 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  

  Fig3: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-CLSTN1 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody ( for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.