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Invitrogen™ MCCC2 Monoclonal Antibody (2B3)

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA522463

Catalog No. PIMA522463


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Description

Description

Peptide Sequence: AYSPRFLYIW PNARISVMGG EQAANVLATI TKDQRAREGK QFSSADEAAL KEPIIKKFEE EGNPYYSSAR VWDDGIIDPA DTRLVLGLSF SAALNAPIEK TDFGIFRM.

COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

MCCC2
Monoclonal
0.5 mg/mL
PBS with no preservative; pH 7.4
Q9HCC0
Mccc2
MCCC2 (NP_071415, 456 a.a. ~ 563 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
100 μg
Primary
Human
Antibody
IgG1 κ
ELISA, Immunohistochemistry (PFA fixed), Western Blot
2B3
Unconjugated
Mccc2
3-methylcrotonyl-CoA carboxylase 2; 3-methylcrotonyl-CoA carboxylase non-biotin-containing subunit; 3-methylcrotonyl-CoA:carbon dioxide ligase subunit beta; 4930552N12Rik; biotin carboxylase; MCCase subunit beta; MCCB; Mccc2; meth; methylcrotonoyl-CoA carboxylase 2; methylcrotonoyl-CoA carboxylase 2 (beta); methylcrotonoyl-CoA carboxylase beta chain, mitochondrial; methylcrotonoyl-Coenzyme A carboxylase 2 (beta); non-biotin containing subunit of 3-methylcrotonyl-CoA carboxylase; testicular secretory protein Li 29
Mouse
Affinity chromatography
RUO
64087
-20°C, Avoid Freeze/Thaw Cycles
Liquid
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