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BCAT1 antibody
The Rabbit Polyclonal anti-BCAT1 antibody is suitable to detect BCAT1 in samples from Human and Mouse. It has been validated for IHC and ELISA.
Catalog No. ABIN7236350
$538.80
Plus shipping costs $50.00
20 μL ABIN7000500
60 μL ABIN7236347
120 μL ABIN7236348
200 μL ABIN7236350
20 μL ABIN7000500
60 μL ABIN7236347
120 μL ABIN7236348
200 μL ABIN7236350
Delivery in 11 to 15 Business Days
Quick Overview for BCAT1 antibody (ABIN7236350)
Target
See all BCAT1 Antibodies
BCAT1
(Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))
Reactivity
All reactivities for BCAT1 antibodies
Human, Mouse
Host
All hosts for BCAT1 antibodies
Rabbit
Clonality
All clonalities for BCAT1 antibodies
Polyclonal
Conjugate
All conjugates for BCAT1 antibodies
This BCAT1 antibody is un-conjugated
Application
All applications for BCAT1 antibodies
Immunohistochemistry (IHC), ELISA
Product Details anti-BCAT1 Antibody
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Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant protein of human BCAT1
Isotype
IgG
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.4 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for BCAT1
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Target
BCAT1
(Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))
Alternative Name
BCAT1
Background
This gene encodes the cytosolic form of the enzyme branched-chain amino acid transaminase. This enzyme catalyzes the reversible transamination of branched-chain alpha-keto acids to branched-chain L-amino acids essential for cell growth. Two different clinical disorders have been attributed to a defect of branched-chain amino acid transamination: hypervalinemia and hyperleucine-isoleucinemia. As there is also a gene encoding a mitochondrial form of this enzyme, mutations in either gene may contribute to these disorders. Alternatively spliced transcript variants have been described.
NCBI Accession
NP_005495
UniProt
P54687
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