3-hydroxyisobutyryl-CoA Hydrolase (HIBCH) (Center) antibody

Antigen: 3-hydroxyisobutyryl-CoA Hydrolase (HIBCH)

Synonyms: HIBYLCOAH, AI648812, MGC31364, 2610509I15Rik, MGC137758, MGC110824, zgc:110824, T11J7.4, T11J7_4, T11J7.5, T11J7_5

Epitope: Center

Clonality: Polyclonal

Host: Rabbit

Reactivity: Human

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Certificates: ISO 9001:2008

Catalog no.: ABIN391638

Additional Information

Characteristics: Purified Rabbit Polyclonal Antibody (Pab)

Alternative name: HIBCH (Center)

Gene ID: 26275

Swiss-Prot: Q6NVY1

Immunogen: This HIBCH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 189~218 amino acids from the Center region of human HIBCH.

Isotype: Ig  (Matching secondary antibodies)

Description: Other names: 3-hydroxyisobutyryl-coenzyme A hydrolase, HIB-CoA hydrolase, HIBYL-CoA-H, 3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, HIBCH

Specificity: This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the Center region of human HIBCH.

Molecular Weight: 43482 DA

Application Details

Application Notes: The suggested dilution is: ELISA ~~ 1:1,000 Western blotting~~ 1:50~100

Concentration: 0.25 mg/ml

Purification: Purified

Buffer: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Storage: Maintain refrigerated at 2-8 deg C for up to 6 months. For long term storage store at -20 deg C in small aliquots to prevent freeze-thaw cycles

Research Area: Cancer, Metabolism, Cell Structure

Restrictions: For Research Use only

Images

Western blot analysis of HIBCH Antibody (Center) (ABIN391638) in K562 cell line lysates (35ug/lane). HIBCH (arrow) was detected using the purified Pab.(2ug/ml)

Formalin-fixed and paraffin-embedded human hepatocarcinoma tissue reacted with HIBCH antibody (Center), which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry. clinical relevance has not been evaluated.