SKU: WR5330 Categories: ,

U-Blot® AID Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR5330-50
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Product details

Background:This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. The protein is involved in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by RefSeq, Feb 2009],

Specifications

TargetAID
ReactivityHuman
ApplicationsWB,IHC,IF,IP,ELISA
MW(Calculated)24kD
MW(Observed)23kD
Host SpeciesRabbit
IsotypeIgG,Kappa
ModificationUnmodified
Recommended Dilution RatioIHC 1:200-1:1000;WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Source
PurificationProtein A
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
ClonalityMonoclonal
Clone NumberPT1564R
SpecificityEndogenous
Gene NameAICDA
Protein NameActivation-induced cytidine deaminase
Other NameAICDA;AID;Activation-induced cytidine deaminase;Cytidine aminohydrolase
Organism-1Human
Gene ID-157379
SwissProt-1Q9GZX7
Organism-2Mouse
Gene ID-211628
SwissProt-2Q9WVE0
Organism-3
Gene ID-3
SwissProt-3
FunctionCatalytic activity:Cytidine + H(2)O = uridine + NH(3).,cofactor:Zinc.,Disease:Defects in AICDA are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2) [MIM:605258]. HIGM2 is characterized by normal or elevated serum IgM levels with absence of IgG, IgA, and IgE, resulting in a profound susceptibility to bacterial infections. HIGM2 causes the absence of Ig class switch recombination (CSR), the lack of Ig somatic hypermutations, and lymph node hyperplasia caused by the presence of giant germinal centers.,Function:RNA-editing deaminase involved in somatic hypermutation, gene conversion, and class-switch recombination. Required for several crucial steps of B-cell terminal differentiation necessary for efficient antibody responses.,online information:AICDA mutation db,similarity:Belongs to the cytidine and deoxycytidylate deaminase family.,tissue specificity:Strongly expressed in lymph nodes and tonsils.,
Cellular LocalizationNucleus . Cytoplasm . Predominantly cytoplasmic (PubMed:21385873). In the presence of MCM3AP/GANP, relocalizes to the nucleus (By similarity). .
Tissue ExpressionStrongly expressed in lymph nodes and tonsils.
Unnamed: 31
SwissProt-3.1
Organism-4
Gene ID-4
SwissProt-4
Cellular Localization.1
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