Monoclonal Antibody to GAPDH (Clone: ABM22C5)

Figure-1: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 0.5 µg/ml on (1) Panc-1, (2) EL-4, (3) Jurkat and (4) HepG2 lysates.

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Figure-1: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 0.5 µg/ml on (1) Panc-1, (2) EL-4, (3) Jurkat and (4) HepG2 lysates.

Figure-2 : Immunohistochemical analysis of GAPDH in human Liver tissue using GAPDH antibody (Clone: ABM22C5) at 3 µg/ml.

Figure-3: Immunohistochemical analysis of GAPDH in human Small intestine tissue using GAPDH antibody (Clone: ABM22C5) at 10 µg/ml.

Figure-4: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 4 µg/ml on (1) CHO-K1 and (2) CHO/PD1 transfected Lysates.

Figure-5: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 4 µg/ml on Raw cell Lysate.

Figure-6: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 1 µg/ml on (1) h Lung, (2) h Testis, (3) h Liver and (4) h Ovary lysates.

Figure-7: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 1 µg/ml on (1) h Brain, (2) m Brain, (3) h Pancrease, (4) h Kidney and (5) m Skeletal Muscle lysates.

Figure-8: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 1 µg/ml on (1) PC3, (2) A549, (3)THP1, (4) Ramos, (5) HCT-116, (6) Raji and (7) MOLT-4 lysates.

Figure-9: Western blot analysis of GAPDH. Anti- GAPDH antibody (Clone: ABM22C5) was used at 1 µg/ml on (1) U937, (2) Saos2, (3) A431, (4) K562, (5) U87, (6) MCF-7, (7) Snu1 and (8) Jurkat lysates.

Product code: 10-10011

Clone name :	ABM22C5
Application :	IHC, WB
Reactivity :	Mouse, Human

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100 µg

$90.00
$260.00

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Download TDS MSDS


Gene :	GAPDH
Gene ID :	2597
Uniprot ID :	P04406
Alternative Name :	GAPDH, GAPD, CDABP0047, OK/SW-cl.12
Format :	Purified
Amount :	100 µg
Isotype :	Mouse IgG1 Kappa
Immunogen Information :	A partial length recombinant GAPDH protein (amino acids 120-320) was used as the immunogen for this antibody.

GAPDH (Glyceraldehyde-3-Phosphate Dehydrogenase) is an enzyme best known for its role in glycolysis. However, extra-glycolytic functions of GAPDH have been described, including regulation of protein expression via RNA binding. GAPDH binds to numerous AREs (adenine-uridine rich elements) from various mRNA 3'-untranslated regions in vitro and in vivo despite its lack of a canonical RNA binding motif. GAPDH specifically catalyzes the simultaneous phosphorylation and oxidation of glyceraldehyde 3-phosphate using NAD+ (Nicotinamide Adenine Dinucleotide) as a cofactor to produce glycerate 1,3-biphosphate and NADH. In addition to its role in energy production, GAPDH has been implicated in many cellular processes including DNA repair tRNA export, membrane fusion and transport, endocytosis and nuclear membrane assembly, and cell death.

Purification :	Protein G Chromatography
Content :	25 µg in 50 µl/100 µg in 200 µl PBS containing 0.05% BSA and 0.05% sodium azide. Sodium azide is highly toxic.
Storage condition :	Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.

Western blot analysis: 0.5-2 µg/ml, Immunohistochemical analysis: 5 µg/ml

For Research Use Only. Not for use in diagnostic/therapeutics procedures.

1. Kakade PS, Budnar S, Kalraiya RD, Vaidya MM. Functional Implications of O-GlcNAcylation-dependent Phosphorylation at a Proximal Site on Keratin 18. J Biol Chem. 2016 Jun 3;291(23):12003-13. doi: 10.1074/jbc.M116.728717. Epub 2016 Apr 8. PubMed PMID: 27059955.

Subcellular location:	Cytoplasm, Nucleus, Cytoplasm, Membrane, Cytoplasm
Post transnational modification:	Oxidative stress can promote the formation of high molecular weight disulfide-linked GAPDH aggregates, through a process called nucleocytoplasmic coagulation. Such aggregates can be observed in vivo in the affected tissues of patients with Alzheimer disease or alcoholic liver cirrhosis, or in cell cultures during necrosis. Oxidation at Met-46 may play a pivotal role in the formation of these insoluble structures. This modification has been detected in vitro following treatment with free radical donor (+/-)-(E)-4-ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide. It has been proposed to destabilize nearby residues, increasing the likelihood of secondary oxidative damages, including oxidation of Tyr-45 and Met-105. This cascade of oxidations may augment GAPDH misfolding, leading to intermolecular disulfide cross-linking and aggregation.
BioGrid:	108868. 205 interactions.