anti-PCBD1 (Center) Antibody

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Catalog number: AP53190PU-N
Price: 587 €
Supplier: acr
Product name: anti-PCBD1 (Center) Antibody
Quantity: 0,4 ml
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More details :

Vial description: DCOHCBDHSterin carbinolamine dehydratase
Category: primary antibody
Raised in: Rabbit
Clone: 1 vial
Form: Affinity Purified
Reactivity: Mouse, Human
Purity: purified
Molecular weight: in kDa
Source: mammalian
Activity: to be determined
Range: broad
Protein number: P61457
Application: Western Blot
Storage: Avoid freeze/thaw cycles, Upon delivery aliquot and store at -20°, C, C for one year, Shipped at 4°
Description: Freeze thaw will destroy a percentage in every cycle and should be avoided, C in a fridge short term in a concentrated dilution, This antibody needs to be stored at + 4°
Properties: C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by acr they should be stored frozen at - 24°
Gene target: PCBD1 (Center)
Short name: anti-PCBD1 (Center) Antibody
Technique: antibodies against human proteins, antibodies for, antibody to, Antibody
Alternative name: antibody to-PCBD1 (central) (Antibody to)
Alternative technique: antibodies
Identity: 8646
Gene: PCBD1 | More about : PCBD1
Long gene name: pterin-4 alpha-carbinolamine dehydratase 1
Synonyms gene: DCOH PCBD
Synonyms gene name: 6-pyruvoyl-tetrahydropterin synthase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1) pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha
Synonyms: PCD
Synonyms name: Pterin-4a-carbinolamine dehydratase (dimerization cofactor of hepatic nuclear factor 1-alpha) pterin-4-alpha carbinolamine dehydratase dimerizing cofactor for HNF1
Locus: 10q22, 1
Discovery year: 1993-06-08
GenBank acession: BC006324
Entrez gene record: 5092
Pubmed identfication: 8486378
RefSeq identity: NM_000281
Havana BLAST/BLAT: OTTHUMG00000018417
Locus Specific Databases: BIOMDBdb: Database of Mutations Causing BH4 Deficiencies and other PND

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