BCAT1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5120441-Each-of-1 | In Stock | ₹ 44,811.50 |
PIPA5120441 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 44,811.50
GST (18%): ₹ 8,066.07
Total Price: ₹ 52,877.57
Antigen
BCAT1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Bcat1
Gene Alias
BCAT(c); Bcat1; BCATC; BCT1; branched chain amino acid transaminase 1; branched chain amino acid transaminase 1, cytosolic; branched chain amino-acid transaminase 1, cytosolic; branched chain aminotransferase 1, cytosolic; branched-chain-amino-acid aminotransferase, cytosolic; cytosolic branched-chain amino acid aminotransferase; Eca39; MECA39; placental protein 18; PNAS121; PP18; Protein ECA39
Host Species
Rabbit
Purification Method
Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
12035, 29592, 586
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Immunocytochemistry, Western Blot
Concentration
1.29 mg/mL
Formulation
PBS with 50% glycerol and 0.01% thimerosal; pH 7.3
Gene Accession No.
P24288, P54687, P54690
Gene Symbols
Bcat1
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 20-190 of human BCAT1 (NP_005495.2).
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Positive test controls include: Jurkat, Raji, SH-SY5Y, Neuro-2a, Mouse brain
- The target is usually found in the following locations: Cytoplasm
- Immunogen sequence: EVVGTFKAKD LIVTPATILK EKPDPNNLVF GTVFTDHMLT VEWSSEFGWE KPHIKPLQNL SLHPGSSALH YAVELFEGLK AFRGVDNKIR LFQPNLNMDR MYRSAVRATL PVFDKEELLE CIQQLVKLDQ EWVPYSTSAS LYIRPTFIGT EPSLGVKKPT KALLFVLLSP V 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.