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SLC25A38 Polyclonal Antibody

Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - SLC25A38 Polyclonal Antibody AP57674
    Sample: bone (Mouse) Lysate at 40 ug
    Primary: Anti-SLC25A38(AP57674)at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution
    Predicted band size: 34kD
    Observed band size: 37kD
  • 14 - SLC25A38 Polyclonal Antibody AP57674
    Paraformaldehyde-fixed, paraffin embedded (Rat stomach); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (SLC25A38) Polyclonal Antibody, Unconjugated (AP57674) at 1:500 overnight at 4°C, followed by a conjugated secondary (sp-0023) for 20 minutes and DAB staining.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P, IHC-F, IF, ICC, E
Primary Accession Q96DW6
Reactivity Rat, Bovine
Host Rabbit
Clonality Polyclonal
Calculated MW 33566 Da
Physical State Liquid
Immunogen KLH conjugated synthetic peptide derived from human SLC25A38
Epitope Specificity 101-200/304
Isotype IgG
Purity affinity purified by Protein A
Buffer 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
SUBCELLULAR LOCATION Mitochondrion inner membrane.
SIMILARITY Belongs to the mitochondrial carrier family. SLC25A38 subfamily. Contains 3 Solcar repeats.
DISEASE Defects in SLC25A38 are a cause of anemia sideroblastic pyridoxine-refractory autosomal recessive (PRARSA) [MIM:205950]. A form of sideroblastic anemia not responsive to pyridoxine. Sideroblastic anemia is characterized by anemia of varying severity, hypochromic peripheral erythrocytes, systemic iron overload secondary to chronic ineffective erythropoiesis, and the presence of bone marrow ringed sideroblasts. Sideroblasts are characterized by iron-loaded mitochondria clustered around the nucleus.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Background Descriptions This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia.[provided by RefSeq, Mar 2010]
Additional Information
Gene ID 54977
Other Names Mitochondrial glycine transporter {ECO:0000255|HAMAP-Rule:MF_03064}, Mitochondrial glycine transporter GlyC, Solute carrier family 25 member 38 {ECO:0000255|HAMAP-Rule:MF_03064}, SLC25A38 {ECO:0000255|HAMAP-Rule:MF_03064}
Target/Specificity Preferentially expressed in erythroid cells.
Dilution WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC=1:100-500,IF=1:100-500,ELISA=1:5000-10000
Format0.01M TBS(pH7.4) with 1% BSA, 0.09% (W/V) sodium azide and 50% Glyce
StorageStore at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Protein Information
Name SLC25A38 (HGNC:26054)
Function Mitochondrial glycine transporter that imports glycine into the mitochondrial matrix. Plays an important role in providing glycine for the first enzymatic step in heme biosynthesis, the condensation of glycine with succinyl-CoA to produce 5-aminolevulinate (ALA) in the mitochondrial matrix. Required during erythropoiesis.
Cellular Location Mitochondrion inner membrane {ECO:0000255|HAMAP- Rule:MF_03064}; Multi-pass membrane protein {ECO:0000255|HAMAP- Rule:MF_03064}
Tissue Location Preferentially expressed in erythroid cells.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

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