SLC25A38 antibody (N-Term)

Catalog No. ABIN5514419

The Rabbit Polyclonal anti-SLC25A38 antibody (ABIN5514419) specifically detects SLC25A38 in WB. The antibody is reactive with Human samples.

Quick Overview for SLC25A38 antibody (N-Term) (ABIN5514419)

Target: SLC25A38 (Solute Carrier Family 25, Member 38 (SLC25A38))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC25A38 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-SLC25A38 Antibody

Binding Specificity: N-Term

Purpose: SLC25A38 Antibody - N-terminal region

Sequence: MIQNSRPSLL QPQDVGDTVE TLMLHPVIKA FLCGSISGTC STLLFQPLDL

Characteristics: This is a rabbit polyclonal antibody against S2538. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human S2538

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Comment:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP74228-100UG

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: prevent freeze-thaw cycles

Storage: 4 °C,-20 °C

Storage Comment: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Target Details for SLC25A38

Target: SLC25A38 (Solute Carrier Family 25, Member 38 (SLC25A38))

Alternative Name: SLC25A38

Background:

Background Information: 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 (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1.

Gene Name: solute carrier family 25 member 38

Alternative Symbols: SIDBA2

Protein Name: mitochondrial glycine transporter

Molecular Weight: 33kDa

Gene ID: 54977

NCBI Accession: NP_060345

UniProt: Q96DW6