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PSMD12 Antibody

Datasheet
Code CSB-PA018902GA01HU
Size $600
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Product Details

Uniprot No.
O00232
Target Names
PSMD12
Alternative Names
26S proteasome non-ATPase regulatory subunit 12 antibody; 26S proteasome regulatory subunit p55 antibody; 26S proteasome regulatory subunit RPN5 antibody; MGC75406 antibody; p55 antibody; proteasome (prosome, macropain) 26S subunit, non ATPase12 antibody; Proteasome 26S non ATPase subunit 12 isoform 2 antibody; PSD12_HUMAN antibody; PSMD12 antibody; Rpn5 antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse,Rat
Immunogen
Human PSMD12
Immunogen Species
Homo sapiens (Human)
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Tested Applications
ELISA,WB,IHC
Protocols
ELISA Protocol
Western Blotting(WB) Protocol
Immunohistochemistry (IHC) Protocol
Troubleshooting and FAQs
Antibody FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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PSMD12 Proteins

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Target Background

Function
Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair.
Gene References into Functions
  1. we identified six de novo genomic deletions and four de novo point mutations in unrelated individuals with intellectual disability, congenital malformations, ophthalmologic anomalies, feeding difficulties, deafness, and subtle dysmorphic facial features PMID: 28132691
Involvement in disease
Stankiewicz-Isidor syndrome (STISS)
Protein Families
Proteasome subunit p55 family
Database Links

HGNC: 9557

OMIM: 604450

KEGG: hsa:5718

STRING: 9606.ENSP00000348442

UniGene: Hs.4295

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