SLC25A38 Polyclonal Antibody
Purified Rabbit Polyclonal Antibody (Pab)
- 产品详情
- 实验流程
Application ![]()
| 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] |
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 |
Format | 0.01M TBS(pH7.4) with 1% BSA, 0.09% (W/V) sodium azide and 50% Glyce |
Storage | Store 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. |
Name | SLC25A38 (HGNC:26054) |
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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.
Application Protocols
Provided below are standard protocols that you may find useful for product applications.

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Cat# AP57674