TBC1D24 Monoclonal antibody, PBS Only

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  WB analysis using 68566-1-Ig (same clone as 68566-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 68566-1-Ig (TBC1D24 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 68566-1-PBS in a different storage buffer formulation.

• 

  WB analysis using 68566-1-Ig (same clone as 68566-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 68566-1-Ig (TBC1D24 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 68566-1-PBS in a different storage buffer formulation.

TBC1D24 Monoclonal Antibody for WB, Indirect ELISA

Cat No. 68566-1-PBS

Clone No.1C7C4

Host / Isotype

Mouse / IgG1

Reactivity

Human, rat, mouse

Applications

WB, Indirect ELISA

Synonyms

KIAA1171, TBC1 domain family member 24, TBC1 domain family, member 24, TBC1D24

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Product Information

68566-1-PBS targets TBC1D24 in WB, Indirect ELISA applications and shows reactivity with Human, rat, mouse samples.

• Tested Reactivity: Human, rat, mouse
• Host / Isotype: Mouse / IgG1
• Class: Monoclonal
• Type: Antibody
• Immunogen: TBC1D24 fusion protein Ag19380
• Full Name: TBC1 domain family, member 24
• Calculated Molecular Weight: 559 aa, 63 kDa
• Observed Molecular Weight: 63 kDa
• GenBank Accession Number: BC127015
• Gene Symbol: TBC1D24
• Gene ID (NCBI): 57465
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Protein G purification
• UNIPROT ID: Q9ULP9
• Storage Buffer: PBS Only
• Storage Conditions: Store at -80°C.

Background Information

TBC1D24 is a protein with a conserved domain, referred to as the TBC domain, characteristic of proteins which interact with GTPases. TBC domain proteins may serve as GTPase-activating proteins for a particular group of GTPases, the Rab (Ras-related proteins in brain) small GTPases which are involved in the regulation of membrane trafficking. Mutations in this gene are associated with familial infantile myoclonic epilepsy.