GALT Antibody (YA2925)

(Synonyms: Gal-1-P uridylyltransferase; UDP-glucose--hexose-1-phosphate uridylyltransferase)
Customer Review

Based on 1 Customer Validation

GALT Antibody (YA2925) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to GALT.

For research use only. We do not sell to patients.
  • Host:

    Rabbit

  • Isotype:

    IgG

  • Application:

    WB, IP

  • Reactivity :

    Human, Mouse, Rat

  • Formulation:

    Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA

  • Conjugation:
    Non-conjugated

Applications

Application
WB Info
WB: Western Blot
IP Info
IP: Immunoprecipitation
Dilution Ratio 1:500-1:1000 1:20

Product Details

Description

GALT Antibody (YA2925) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to GALT.

  • Host Rabbit
  • Clonality Recombinant,Monoclonal
  • Species Reactivity
    Human, Mouse, Rat
  • Observed Molecular Weight
    Observed band size: 43 kDa Info
    Note: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
  • Calculated Molecular Weight Predicted band size: 43 kDa
Immunogen

A synthetic peptide of human GALT

Sensitivity

Endogenous

Purification

Affinity Purified

Conjugation

Non-conjugated

Modification

Unmodified

Isotype

IgG

RRID

AB_3105295

Product Properties

  • Appearance

    Solution

  • Formulation

    Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA

  • Concentration

    Batch-dependent, Please check the COA for the concentration of each lot. Check Lot Concentration

  • Storage & Stability

    Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

  • Shipping

    Shipping with blue ice.

Verification Images

  • Experimental Validation Results for GALT Antibody (YA2925)
    Western blot analysis was performed on extracts from K562 (lane 1, 15 μg), HepG2 (lane 2, 15 μg), Hela (lane 3, 15 μg), C6 (lane 4, 15 μg), Mouse liver (lane 5, 15 μg), and Rat brain (lane 6, 15 μg) using GALT Rabbit mAb.Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST at 4°C overnight.The primary antibody (1:1000 dilution) and the loading control antibody (GAPDH, HY-P80137, 1:40000 dilution) were incubated in 5% non-fat milk in TBST for 1 hour at 37°C.Goat Anti-Rabbit IgG-HRP Secondary Antibody (1:20000 dilution) was then applied for 40 minutes at 37°C.
  • Experimental Validation Results for GALT Antibody (YA2925)
    Western blot analysis of extracts from Hela(lane 2(20ug) , C6(lane 3(20ug) and HEK293(lane 4(20ug) using GALT Antibody (HY-P83180) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P83730, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

Background

  • Function

    GALT encodes galactose-1-phosphate uridylyltransferase, a homodimeric HIT protein superfamily enzyme that catalyzes the second Leloir pathway step, converting galactose-1-phosphate and UDP-glucose into glucose-1-phosphate and UDP-galactose[1]. Mechanistically, GALT acts after GALM and GALK1 and before GALE, placing it at the central transferase step of galactose metabolism[1][2]. GALT deficiency causes classic galactosemia, a neonatal metabolic disease that can present as life-threatening illness and remains associated with long-term cognitive, social, and reproductive complications despite dietary galactose restriction[3]. In disease models, GALT-deficient mice showed absent GALT activity, reduced litter size, delayed pregnancy, and growth restriction, supporting their use for pathogenesis and therapy studies[4]. Compared with related Leloir enzymes, GALT differs from ATP-dependent GALK1 and SDR-family GALE because it functions as a HIT-family uridylyltransferase with a His-Pro-His active-site motif[1]. Compared with Duarte GALT variants, classic galactosemia shows very low residual GALT activity, whereas Duarte alleles retain partial enzyme function[1][3]. For experimental applications, mutant GALT studies link enzymatic impairment to altered substrate binding, thermal stability, and folding, supporting pharmacological chaperones and proteostasis regulators as research directions[5].- GALT defines the HIT-family transferase step connecting galactose-1-phosphate clearance with UDP-galactose production[1].- Classic galactosemia models support mechanistic studies of fertility, growth, neurological outcomes, and therapy[3][4].- Mutant GALT folding assays provide practical tools for evaluating chaperone-based rescue strategies[5].

  • Isoforms & Post-Translational Modification

    P07902 has 2 isomers: P07902-1: 43363 Da (predicted); P07902-2: 31107 Da (predicted).

  • Subunit

    Homodimer

  • SwissProt ID

    P07902

  • Gene ID
  • Synonyms

    Gal-1-P uridylyltransferase; UDP-glucose--hexose-1-phosphate uridylyltransferase

  • Research Field

    Signal Transduction

References

GALT Antibody (YA2925) Related Classifications

MOQ
Minimum order quantity
100 mg

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