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Anti-CD40 Rabbit pAb

Purified Rabbit Polyclonal Antibody

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货号 规格 价格
P100046
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-CD40 Rabbit pAb
Anti-CD40 Rabbit pAb
Anti-CD40 Rabbit pAb
Product NameAnti-CD40 Rabbit pAb
DescriptionPurified Rabbit Polyclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P/IF (Tissue-P), IF (Cell)/ICC, ELISA
DilutionWB 1:500~1:1,000; IHC-P 1:50~1:200; IF 1:50~1:200
ReactivityHuman, Mouse
HostRabbit
ClonalityPolyclonal
IsotypeIgG
LabelUnconjugated
ImmunogenRecombinant fusion protein containing a sequence within amino acids 198-277 of human CD40 (NP_001241.1).
FormatAffinity purified polyclonal antibody supplied in PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Synonymsp50; Bp50; CDW40; TNFRSF5; CD40.
Molecular weightCalculated MW: 31 kDa; Observed MW: 45 kDa
Uniprot ID P25942
Gene ID 958
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-CD40 Rabbit pAb is for research use only and not for use in diagnostic or therapeutic procedures.
Background This gene is a member of the TNF-receptor superfamily. The encoded protein is a receptor on antigen-presenting cells of the immune system and is essential for mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3). Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported.

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