ALDH4A1 Mouse Monoclonal Antibody (HRP conjugated) [Clone ID: OTI1H10]

CAT#: TA812719BM

ALDH4A1 mouse monoclonal antibody,clone OTI1H10, HRP conjugated

Conjugation: Unconjugated Biotin HRP



  View other "OTI1H10" antibodies (4)

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CNY 3,990.00


货期*
2周

规格
    • 100 ul

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Transient overexpression lysate of aldehyde dehydrogenase 4 family, member A1 (ALDH4A1), nuclear gene encoding mitochondrial protein, transcript variant P5CDhS
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Specifications

Product Data
Clone Name OTI1H10
Applications IHC, WB
Recommend Dilution WB 1:500, IHC 1:500
Reactivity Human, Dog, Rat, Mouse
Host Mouse
Clonality Monoclonal
Immunogen Human recombinant protein fragment corresponding to amino acids 1-503 of human ALDH4A1 (NP_001154976) produced in E.coli.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol.
Concentration 0.5 mg/ml
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation HRP
Storage Condition Store at -20°C as received.
Gene Name aldehyde dehydrogenase 4 family member A1
Background This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2009]
Synonyms ALDH4; P5CD; P5CDh
Reference Data
Protein Families Druggable Genome
Protein Pathways Alanine, aspartate and glutamate metabolism, Arginine and proline metabolism, Metabolic pathways
*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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