PEX5 Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI1D3]

CAT#: TA501389AM

Anti-PEX5 mouse monoclonal antibody, clone OTI1D3 (formerly 1D3), Biotinylated

Conjugation: Unconjugated Biotin HRP



  View other "OTI1D3" antibodies (4)

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CNY 3,990.00


货期*
2周

规格
    • 100 ul

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经常一起买 (3)
beta Actin Mouse Monoclonal Antibody, Clone OTI1, Loading Control
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Recombinant protein of human peroxisomal biogenesis factor 5 (PEX5), transcript variant 2, 20 µg
    • 20 ug

CNY 2,900.00
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Transient overexpression lysate of peroxisomal biogenesis factor 5 (PEX5), transcript variant 2
    • 100 ug

CNY 3,080.00

Specifications

Product Data
Clone Name OTI1D3
Applications IF, WB
Recommend Dilution WB 1:2000, IF 1:100
Reactivity Human, Dog, Mouse, Rat
Host Mouse
Clonality Monoclonal
Immunogen Full length human recombinant protein of human PEX5 (NP_000310) produced in HEK293T cell.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Concentration 0.5 mg/ml
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Biotin
Storage Condition Store at -20°C as received.
Predicted Protein Size 69.7 kDa
Gene Name peroxisomal biogenesis factor 5
Background The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq]
Synonyms PBD2A; PBD2B; PTS1-BP; PTS1R; PXR1; RCDP5
Reference Data
Protein Families Druggable Genome
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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